Canonical Allele Identifier: PA1139747353
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 853419
ClinVar RCV Id: RCV001058220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Gly175Trp
CA402994349
NM_138924.3:c.523G>T