Canonical Allele Identifier: PA1139732660
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 857063
ClinVar RCV Id: RCV001062669 RCV002553925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066970.3:p.His242Tyr
CA359721345
NM_021147.5:c.724C>T