Canonical Allele Identifier: PA658664124
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 454919
ClinVar RCV Id: RCV000541138
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066970.3:p.Leu282Pro
CA3266665
NM_021147.5:c.845T>C