Allele Registry

Canonical Allele Identifier: PA2826195816

Gene: CEP152 HGNC NCBI

ClinVar RCV:

RCV000303990

RCV000391854

RCV002502233

RCV002520965

RCV004537784

ClinVar Variation:

316415

HGVS (amino-acid)	Matching Registered Transcripts
NP_001181927.1:p.Pro1145Thr	CA7548347 NM_001194998.2:c.3433C>A