Canonical Allele Identifier: PA2825068247
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1462940
ClinVar RCV Id: RCV001960804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Gly13Ala
CA402998398
NM_000156.6:c.38G>C