Canonical Allele Identifier: PA2828278066
Gene: CEP83 HGNC NCBI

Linked Data

ClinVar Variation Id: 392913
ClinVar RCV Id: RCV000417742 RCV001034799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354966.1:p.Arg441Gly
CA6721683
NM_001368037.1:c.1321A>G