Canonical Allele Identifier: PA916058038
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 644509
ClinVar RCV Id: RCV000798445 RCV004027958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066970.3:p.Asn21Ser
CA3266873
NM_021147.5:c.62A>G