Canonical Allele Identifier: PA658806489
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 525346
ClinVar RCV Id: RCV000629400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066970.3:p.Lys188Arg
CA359722594
NM_021147.5:c.563A>G