Canonical Allele Identifier: PA2573284023
Gene: CEP97 HGNC NCBI

Linked Data

ClinVar Variation Id: 1528284
ClinVar RCV Id: RCV002077468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078824.2:p.Val408Phe
CA2522094
NM_024548.4:c.1222G>T