Canonical Allele Identifier: PA915984485
Gene: GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 37357

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245261.1:p.His23Tyr
CA259382
NM_001258332.2:c.67C>T