Canonical Allele Identifier: PA092279
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 25298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000146.2:p.Ala320Thr
CA259544
NM_000155.4:c.958G>A