Canonical Allele Identifier: PA645434605
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 416791
ClinVar RCV Id: RCV000473732 RCV000660536 RCV001311652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066970.3:p.Pro45His
CA3266854
NM_021147.5:c.134C>A