Allele Registry

Canonical Allele Identifier: PA115686

Gene: A4GALT HGNC NCBI

ClinVar Allele:

17732

ClinVar RCV:

RCV000002812

RCV003546450

ClinVar Variation:

2693

HGVS (amino-acid)	Matching Registered Transcripts
NP_059132.1:p.Pro251Leu	CA115685 NM_017436.7:c.752C>T