Allele Registry

Canonical Allele Identifier: PA645434605

Gene: CCNO HGNC NCBI

ClinVar RCV:

RCV000473732

RCV000660536

RCV001311652

ClinVar Variation:

416791

HGVS (amino-acid)	Matching Registered Transcripts
NP_066970.3:p.Pro45His	CA3266854 NM_021147.5:c.134C>A