Canonical Allele Identifier: PA891845839
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 588631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Trp20Leu
CA402998326
NM_000156.6:c.59G>T