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MMAA - metabolism of cobalamin associated A

  • Synonym(s) : cblA
  • Previous symbols and names : methylmalonic aciduria (cobalamin deficiency) cblA type, methylmalonic aciduria (cobalamin deficiency) type A
  • Type : gene with protein product
  • Chromosomal location : 4q31.21
  • OMIM: 607481
  • HGNC: 18871
  • UniProtKB: Q8IVH4
  • Genatlas: MMAA
  • Ensembl: ENSG00000151611
  • IUPHAR-DB: -
  • Reactome: Q8IVH4
  • LOVD: MMAA

Diseases list

  : Assessed

Additional information

Health care resources for this gene

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