Canonical Allele Identifier: PA658806903
Gene: CSNK2B HGNC NCBI

Linked Data

ClinVar Variation Id: 520596
ClinVar RCV Id: RCV000624714 RCV001249735 RCV002221564 RCV001860419 RCV003411469 RCV003139949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311.3:p.Asp32Asn
CA363471803
NM_001320.7:c.94G>A