Allele Registry

Canonical Allele Identifier: PA115690

Gene: A4GALT HGNC NCBI

ClinVar Allele:

17734

ClinVar RCV:

RCV000002814

ClinVar Variation:

2695

HGVS (amino-acid)	Matching Registered Transcripts
NP_059132.1:p.Gly187Asp	CA115689 NM_017436.7:c.560G>A