Canonical Allele Identifier: PA658676469
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 478015

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Arg158His
CA9043633
NM_000156.6:c.473G>A