Canonical Allele Identifier: PA645434610
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 411594
ClinVar RCV Id: RCV000470093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066970.3:p.Leu213Pro
CA3266707
NM_021147.5:c.638T>C