Canonical Allele Identifier: PA658664128
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 454920
ClinVar RCV Id: RCV000551760 RCV003314606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066970.3:p.Ile326Met
CA359720502
NM_021147.5:c.978A>G