Allele Registry

Canonical Allele Identifier: PA171729

Gene: CEP152 HGNC NCBI

ClinVar RCV:

RCV000145626

RCV000273027

RCV000330394

RCV000967357

ClinVar Variation:

158254

HGVS (amino-acid)	Matching Registered Transcripts
NP_001181927.1:p.Val1106Ala	CA171728 NM_001194998.2:c.3317T>C