Allele Registry

Canonical Allele Identifier: PA658654834

Gene: CEP120 HGNC NCBI

ClinVar Allele:

439493

ClinVar RCV:

RCV000515151

ClinVar Variation:

446146

HGVS (amino-acid)	Matching Registered Transcripts
NP_694955.2:p.Leu726Pro	CA360898838 NM_153223.4:c.2177T>C