Canonical Allele Identifier: PA2580424501
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 2388009
ClinVar RCV Id: RCV002729762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066970.3:p.Ser63Tyr
CA3266841
NM_021147.5:c.188C>A