Canonical Allele Identifier: PA2825068328
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2446455
ClinVar RCV Id: RCV003159289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Ala57Asp
CA402998003
NM_000156.6:c.170C>A