Allele Registry

Canonical Allele Identifier: PA916014639

Gene: CETP HGNC NCBI

ClinVar Allele:

343500

ClinVar RCV:

RCV000371616

RCV000966006

ClinVar Variation:

319970

HGVS (amino-acid)	Matching Registered Transcripts
NP_001273014.1:p.Ala15Gly	CA8070732 NM_001286085.2:c.44C>G