Canonical Allele Identifier: PA1139732565
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 846075
ClinVar RCV Id: RCV001049282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066970.3:p.Gly70Ser
CA359724963
NM_021147.5:c.208G>A