Canonical Allele Identifier: PA2573280510
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 1362575
ClinVar RCV Id: RCV001900229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066970.3:p.Glu62Gly
CA359725115
NM_021147.5:c.185A>G