Canonical Allele Identifier: PA2580309850
Gene: CCNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2210366
ClinVar RCV Id: RCV004074908
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004692.1:p.Val387Ile
CA7588886
NM_004701.4:c.1159G>A