Canonical Allele Identifier: PA2825068494
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1020905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.His155Asp
CA402994771
NM_000156.6:c.463C>G