Allele Registry

Canonical Allele Identifier: PA2828796558

Gene: CC2D2A HGNC NCBI

ClinVar Allele:

214178

ClinVar RCV:

RCV000201741

RCV003765303

ClinVar Variation:

217601

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365544.1:p.Val1045Ala	CA279522 NM_001378615.1:c.3134T>C