Canonical Allele Identifier: PA2741988015
Gene: CEP97 HGNC NCBI

Linked Data

ClinVar Variation Id: 2995734
ClinVar RCV Id: RCV003853821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078824.2:p.Ile493Val
CA2522136
NM_024548.4:c.1477A>G