Allele Registry

Canonical Allele Identifier: PA097793

Gene: CC2D2A HGNC NCBI

ClinVar Allele:

39891

ClinVar RCV:

RCV000023923

RCV000594523

RCV001852033

RCV004532401

ClinVar Variation:

30934

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073991.2:p.Glu1447Ala	CA129547 NM_001080522.2:c.4340A>C