Canonical Allele Identifier: PA2826882022
Gene: CEP97 HGNC NCBI

Linked Data

ClinVar Variation Id: 2920540
ClinVar RCV Id: RCV003736328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290330.1:p.Asp755Glu
CA2522325
NM_001303401.2:c.2265C>A
CA353882124
NM_001303401.2:c.2265C>G