Canonical Allele Identifier: PA2829967611
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 3139985
ClinVar RCV Id: RCV004430809
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066970.3:p.Ile57Val
CA359725243
NM_021147.5:c.169A>G