Allele Registry

Canonical Allele Identifier: PA2826027428

Gene: CEP120 HGNC NCBI

ClinVar RCV:

RCV000515151

ClinVar Variation:

446146

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159698.1:p.Leu700Pro	CA360898838 NM_001166226.2:c.2099T>C