Canonical Allele Identifier: PA915984662
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 25222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245261.1:p.Leu86Pro
CA342595
NM_001258332.2:c.257T>C