Canonical Allele Identifier: PA2828278029
Gene: CEP83 HGNC NCBI

Linked Data

ClinVar Variation Id: 381892

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354966.1:p.Asp373Val
CA6721749
NM_001368037.1:c.1118A>T