Canonical Allele Identifier: PA2828278432
Gene: CEP83 HGNC NCBI

Linked Data

ClinVar Variation Id: 139544
ClinVar RCV Id: RCV000128443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354967.1:p.Arg511Pro
CA163253
NM_001368038.1:c.1532G>C