Canonical Allele Identifier: PA658826369
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 546535
ClinVar RCV Id: RCV000658429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Leu177Val
CA402994325
NM_000156.6:c.529C>G