Allele Registry

Canonical Allele Identifier: PA645434610

Gene: CCNO HGNC NCBI

ClinVar Allele:

395335

ClinVar RCV:

RCV000470093

ClinVar Variation:

411594

HGVS (amino-acid)	Matching Registered Transcripts
NP_066970.3:p.Leu213Pro	CA3266707 NM_021147.5:c.638T>C