Canonical Allele Identifier: PA2825068462
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2446459
ClinVar RCV Id: RCV003159293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Asp135Tyr
CA402995388
NM_000156.6:c.403G>T