Canonical Allele Identifier: PA645434612
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 411595
ClinVar RCV Id: RCV000457600 RCV003418200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066970.3:p.Gly229Ser
CA3266705
NM_021147.5:c.685G>A