Allele Registry

Canonical Allele Identifier: PA2828787219

Gene: CC2D2A HGNC NCBI

ClinVar Allele:

292625

ClinVar RCV:

RCV000284136

RCV000320497

RCV000379227

RCV001315843

RCV001753820

ClinVar Variation:

347842

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365546.1:p.Phe862Leu	CA2863998 NM_001378617.1:c.2584T>C CA356412335 NM_001378617.1:c.2586T>A CA356412336 NM_001378617.1:c.2586T>G