Canonical Allele Identifier: PA645482146
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 429489

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.His51Asp
CA402998055
NM_000156.6:c.151C>G