Allele Registry

Canonical Allele Identifier: PA2828591670

Gene: CEP120 HGNC NCBI

ClinVar Allele:

439491

ClinVar RCV:

RCV000515139

ClinVar Variation:

446144

HGVS (amino-acid)	Matching Registered Transcripts
NP_001362336.1:p.Val194Ala	CA360893331 NM_001375407.1:c.581T>C