Allele Registry

Canonical Allele Identifier: PA097829

Gene: CC2D2A HGNC NCBI

ClinVar Allele:

191984

ClinVar RCV:

RCV000175282

RCV000860615

RCV000987417

RCV001147192

RCV003436969

ClinVar Variation:

194821

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073991.2:p.Pro721Ser	CA201373 NM_001080522.2:c.2161C>T