Canonical Allele Identifier: PA2580462386
Gene: CEP97 HGNC NCBI

Linked Data

ClinVar Variation Id: 2071650
ClinVar RCV Id: RCV002975748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078824.2:p.Pro344Leu
CA2522059
NM_024548.4:c.1031C>T