Canonical Allele Identifier: PA2499249422
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_001311.3:p.Phe34Cys
CA363471873
NM_001320.7:c.101T>G