Canonical Allele Identifier: PA2826643455
Gene: CSNK2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1275774
ClinVar RCV Id: RCV001682651
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269314.1:p.Phe34Cys
CA363471873
NM_001282385.2:c.101T>G