Allele Registry

Canonical Allele Identifier: PA2826703604

Gene: CETP HGNC NCBI

ClinVar RCV:

RCV000019077

RCV000283037

RCV001636604

RCV001699101

RCV002243654

ClinVar Variation:

17525

HGVS (amino-acid)	Matching Registered Transcripts
NP_001273014.1:p.Val362Ile	CA127242 NM_001286085.2:c.1084G>A CA3047141823 NM_001286085.2:c.1083_1084delinsAA