Allele Registry

Canonical Allele Identifier: PA2826703649

Gene: CETP HGNC NCBI

ClinVar RCV:

RCV000032602

RCV001560193

ClinVar Variation:

17527

HGVS (amino-acid)	Matching Registered Transcripts
NP_001273014.1:p.Asp399Gly	CA130258 NM_001286085.2:c.1196A>G