Canonical Allele Identifier: PA916058040
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 648428
ClinVar RCV Id: RCV000803152 RCV003746555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066970.3:p.Ser63Pro
CA3266843
NM_021147.5:c.187T>C