Canonical Allele Identifier: PA916071400
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 546535
ClinVar RCV Id: RCV000658429
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Leu177Val
CA402994325
NM_138924.3:c.529C>G