Allele Registry

Canonical Allele Identifier: PA2826976879

Gene: A4GALT HGNC NCBI

ClinVar Allele:

17732

ClinVar RCV:

RCV000002812

RCV003546450

ClinVar Variation:

2693

HGVS (amino-acid)	Matching Registered Transcripts
NP_001304967.1:p.Pro251Leu	CA115685 NM_001318038.3:c.752C>T