Canonical Allele Identifier: PA658806512
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 525497
ClinVar RCV Id: RCV000629570
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066970.3:p.Pro336Leu
CA3266637
NM_021147.5:c.1007C>T