Canonical Allele Identifier: PA2826881950
Gene: CEP97 HGNC NCBI

Linked Data

ClinVar Variation Id: 2165320
ClinVar RCV Id: RCV003089917
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290330.1:p.Leu442Pro
CA2522140
NM_001303401.2:c.1325T>C