Canonical Allele Identifier: PA092357
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 37359

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000146.2:p.Arg148Trp
CA259393
NM_000155.4:c.442C>T