Canonical Allele Identifier: PA2826976841
Gene: A4GALT HGNC NCBI

Linked Data

ClinVar Variation Id: 2057176
ClinVar RCV Id: RCV002923220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304967.1:p.Ser100Leu
CA10270337
NM_001318038.3:c.299C>T