Canonical Allele Identifier: PA2573073710
Gene: CEP120 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362338.1:p.Val3Ala
CA360893331
NM_001375409.1:c.8T>C