Canonical Allele Identifier: PA2826613466
Gene: CEP43 HGNC NCBI

Linked Data

ClinVar Variation Id: 3142945
ClinVar RCV Id: RCV004436330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265619.1:p.Lys165Gln
CA366409112
NM_001278690.2:c.493A>C