Canonical Allele Identifier: PA645434625
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 416793
ClinVar RCV Id: RCV000473019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066970.3:p.Gly264Arg
CA3266680
NM_021147.5:c.790G>C
CA359721146
NM_021147.5:c.790G>A