Canonical Allele Identifier: PA2826976848
Gene: A4GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 718696
ClinVar RCV Id: RCV000891686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304967.1:p.Ser123Pro
CA10270322
NM_001318038.3:c.367T>C