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SLC6A19 - solute carrier family 6 member 19

  • Synonym(s) : Hartnup disease
  • Previous symbols and names : solute carrier family 6 (neutral amino acid transporter), member 19
  • Type : gene with protein product
  • Chromosomal location : 5p15.33
  • OMIM: 608893
  • HGNC: 27960
  • UniProtKB: Q695T7
  • Genatlas: SLC6A19
  • Ensembl: ENSG00000174358
  • IUPHAR-DB: -
  • Reactome: Q695T7
  • LOVD: SLC6A19

Diseases list

  : Assessed

Additional information

Health care resources for this gene

Specialised Social Services

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