Search for a gene
BRAF - B-Raf proto-oncogene, serine/threonine kinase
Diseases list
- Disease-causing germline mutation(s) in Noonan syndrome with multiple lentigines
ORPHA:500 
- Disease-causing germline mutation(s) (gain of function) in Cardiofaciocutaneous syndrome
ORPHA:1340 - Disease-causing somatic mutation(s) in Classic hairy cell leukemia
ORPHA:58017 - Disease-causing somatic mutation(s) in Craniopharyngioma
ORPHA:54595 - Disease-causing somatic mutation(s) in Cushing disease
ORPHA:96253 - Disease-causing somatic mutation(s) in Differentiated thyroid carcinoma
ORPHA:146 - Disease-causing somatic mutation(s) in Langerhans cell histiocytosis
ORPHA:389 - Disease-causing somatic mutation(s) in Large congenital melanocytic nevus
ORPHA:626 - Disease-causing somatic mutation(s) in NON RARE IN EUROPE: Melanoma
ORPHA:411533 - Disease-causing somatic mutation(s) in Pilomyxoid astrocytoma
ORPHA:251615 - Disease-causing somatic mutation(s) in Syringocystadenoma papilliferum
ORPHA:840 - Part of a fusion gene in Large congenital melanocytic nevus
ORPHA:626 - Part of a fusion gene in Pilomyxoid astrocytoma
ORPHA:251615
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
Orphanet is part of the Gene Curation Coalition, a global effort to harmonise gene-level resources.