Allele Registry

Canonical Allele Identifier: PA2828788355

Gene: CC2D2A HGNC NCBI

ClinVar RCV:

RCV000201684

ClinVar Variation:

217603

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365546.1:p.Thr1532Ala	CA279482 NM_001378617.1:c.4594A>G