Canonical Allele Identifier: PA2828279203
Gene: CEP83 HGNC NCBI

Linked Data

ClinVar Variation Id: 381892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354970.1:p.Asp298Val
CA6721749
NM_001368041.1:c.893A>T