Canonical Allele Identifier: PA2828279269
Gene: CEP83 HGNC NCBI

Linked Data

ClinVar Variation Id: 139544
ClinVar RCV Id: RCV000128443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354970.1:p.Arg436Pro
CA163253
NM_001368041.1:c.1307G>C