Canonical Allele Identifier: PA2827373696
Gene: CEP83 HGNC NCBI

Linked Data

ClinVar Variation Id: 381892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333387.1:p.Asp269Val
CA6721749
NM_001346458.2:c.806A>T