Canonical Allele Identifier: PA658676457
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 449690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Gln106Pro
CA9043739
NM_000156.6:c.317A>C