Canonical Allele Identifier: PA2826467780
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 25298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245261.1:p.Ala211Thr
CA259544
NM_001258332.2:c.631G>A