Canonical Allele Identifier: PA891848999
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 570940
ClinVar RCV Id: RCV000691939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066970.3:p.Gly56Ser
CA359725269
NM_021147.5:c.166G>A