Canonical Allele Identifier: PA2573198135
Gene: CSNK2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1690342
ClinVar RCV Id: RCV002251812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311.3:p.Leu36Pro
CA363471919
NM_001320.7:c.107T>C