Canonical Allele Identifier: PA2829355767
Gene: CSNK2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 224790
ClinVar RCV Id: RCV000210367 RCV000239482 RCV001267578 RCV001420211 RCV002273990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001886.1:p.Lys198Arg
CA358394
NM_001895.4:c.593A>G