Canonical Allele Identifier: PA2826613474
Gene: CEP43 HGNC NCBI

Linked Data

ClinVar Variation Id: 3142952
ClinVar RCV Id: RCV004436337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265619.1:p.Leu270Val
CA4095589
NM_001278690.2:c.808C>G