Canonical Allele Identifier: PA2825068476
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1476786
ClinVar RCV Id: RCV001998211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Thr143Ile
CA9043663
NM_000156.6:c.428C>T