Canonical Allele Identifier: PA658676426
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 449597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Ile9Val
CA402998450
NM_000156.6:c.25A>G