Allele Registry

Canonical Allele Identifier: PA203499

Gene: CCDC22 HGNC NCBI

ClinVar RCV:

RCV000179938

RCV000886329

ClinVar Variation:

198556

HGVS (amino-acid)	Matching Registered Transcripts
NP_054727.1:p.Glu239Lys	CA203498 NM_014008.5:c.715G>A