Allele Registry

Canonical Allele Identifier: PA110502

Gene: CEP152 HGNC NCBI

ClinVar RCV:

RCV000024028

RCV000145604

RCV000968712

ClinVar Variation:

31034

HGVS (amino-acid)	Matching Registered Transcripts
NP_001181927.1:p.Lys667Arg	CA129630 NM_001194998.2:c.2000A>G