Canonical Allele Identifier: PA658676452
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 450527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Arg98Gln
CA9043746
NM_000156.6:c.293G>A