Allele Registry

Canonical Allele Identifier: PA645414061

Gene: CR2 HGNC NCBI

ClinVar RCV:

RCV000455766

RCV001511020

RCV001618686

ClinVar Variation:

402560

HGVS (amino-acid)	Matching Registered Transcripts
NP_001006659.1:p.Ser663Pro	CA1368857 NM_001006658.3:c.1987T>C