Canonical Allele Identifier: PA2580309845
Gene: CCNB2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004692.1:p.Asp232Ala
CA392640532
NM_004701.4:c.695A>C