Canonical Allele Identifier: PA2828592009
Gene: CEP120 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362337.1:p.Leu535Pro
CA360898838
NM_001375408.1:c.1604T>C