Canonical Allele Identifier: PA645510007
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 25180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245261.1:p.Val42Ala
CA259396
NM_001258332.2:c.125T>C