Allele Registry

Canonical Allele Identifier: PA2828787576

Gene: CC2D2A HGNC NCBI

ClinVar RCV:

RCV001985408

ClinVar Variation:

1446135

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365546.1:p.Arg1051Cys	CA2864139 NM_001378617.1:c.3151C>T