Canonical Allele Identifier: PA2829355743
Gene: CSNK2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 619014
ClinVar RCV Id: RCV000757921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001886.1:p.Asp156His
CA407933108
NM_001895.4:c.466G>C