Canonical Allele Identifier: PA2580510338
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1989243
ClinVar RCV Id: RCV002786407

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Ala56Thr
CA402998018
NM_138924.3:c.166G>A