Canonical Allele Identifier: PA2827373402
Gene: CEP83 HGNC NCBI

Linked Data

ClinVar Variation Id: 381892
ClinVar RCV Id: RCV001035539 RCV000434526 RCV003983042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333386.1:p.Asp373Val
CA6721749
NM_001346457.2:c.1118A>T