Canonical Allele Identifier: PA2828064857
Gene: CSNK2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 421395
ClinVar RCV Id: RCV000479609 RCV001249615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349700.1:p.Asp156Glu
CA16620934
NM_001362771.2:c.468T>A
CA407933096
NM_001362771.2:c.468T>G