Allele Registry

Canonical Allele Identifier: PA097675

Gene: CETP HGNC NCBI

ClinVar Allele:

32566

ClinVar RCV:

RCV000032602

RCV001560193

ClinVar Variation:

17527

HGVS (amino-acid)	Matching Registered Transcripts
NP_000069.2:p.Asp459Gly	CA130258 NM_000078.3:c.1376A>G