Canonical Allele Identifier: PA314821
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205588
ClinVar RCV Id: RCV000793466 RCV002354525 RCV001704993
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Ala196Val
CA314820
NM_000156.6:c.587C>T