Canonical Allele Identifier: PA658801443
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 544257

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Thr136Met
CA9043669
NM_000156.6:c.407C>T