Canonical Allele Identifier: PA916071379
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 429874
ClinVar RCV Id: RCV000493155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Tyr168Ser
CA402994540
NM_138924.3:c.503A>C