Canonical Allele Identifier: PA2826976846
Gene: A4GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 1346328
ClinVar RCV Id: RCV002029955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304967.1:p.Val112Ile
CA10270328
NM_001318038.3:c.334G>A