Allele Registry

Canonical Allele Identifier: PA2828787569

Gene: CC2D2A HGNC NCBI

ClinVar RCV:

RCV002785636

ClinVar Variation:

1982871

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365546.1:p.Val1050Leu	CA356418571 NM_001378617.1:c.3148G>C CA356418573 NM_001378617.1:c.3148G>T