Canonical Allele Identifier: PA2825068316
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1059226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Ala52Thr
CA304067259
NM_000156.6:c.154G>A