Canonical Allele Identifier: PA2826643458
Gene: CSNK2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2229410
ClinVar RCV Id: RCV002712549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269314.1:p.Leu39Pro
CA363471999
NM_001282385.2:c.116T>C