Allele Registry

Canonical Allele Identifier: PA2828788073

Gene: CC2D2A HGNC NCBI

ClinVar RCV:

RCV000201617

ClinVar Variation:

217609

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365546.1:p.Ile1360Thr	CA279416 NM_001378617.1:c.4079T>C