Canonical Allele Identifier: PA645420744
Gene: CEP83 HGNC NCBI

Linked Data

ClinVar Variation Id: 381892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057206.2:p.Asp373Val
CA6721749
NM_016122.3:c.1118A>T