Canonical Allele Identifier: PA295621
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 167131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Tyr27His
CA295620
NM_000156.6:c.79T>C