Allele Registry

Canonical Allele Identifier: PA658806489

Gene: CCNO HGNC NCBI

ClinVar RCV:

RCV000629400

ClinVar Variation:

525346

HGVS (amino-acid)	Matching Registered Transcripts
NP_066970.3:p.Lys188Arg	CA359722594 NM_021147.5:c.563A>G