Canonical Allele Identifier: PA314845
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1766473
ClinVar RCV Id: RCV002371514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Asp31Val
CA314844
NM_000156.6:c.92A>T