Canonical Allele Identifier: PA2580424518
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 2339985
ClinVar RCV Id: RCV002960161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066970.3:p.Ala260Ser
CA359721176
NM_021147.5:c.778G>T