Allele Registry

Canonical Allele Identifier: PA2828786626

Gene: CC2D2A HGNC NCBI

ClinVar RCV:

RCV000335348

RCV001149502

RCV001149503

RCV001248140

RCV002487294

RCV002518166

RCV004537623

ClinVar Variation:

291191

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365546.1:p.Thr515Met	CA2863732 NM_001378617.1:c.1544C>T