Canonical Allele Identifier: PA2828278949
Gene: CEP83 HGNC NCBI

Linked Data

ClinVar Variation Id: 392913

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354969.1:p.Arg337Gly
CA6721683
NM_001368040.1:c.1009A>G