Allele Registry

Canonical Allele Identifier: PA110488

Gene: CEP152 HGNC NCBI

ClinVar RCV:

RCV000000072

RCV000413650

RCV000763360

RCV000778440

ClinVar Variation:

HGVS (amino-acid)	Matching Registered Transcripts
NP_001181927.1:p.Gln265Pro	CA210936 NM_001194998.2:c.794A>C