Canonical Allele Identifier: PA2828064759
Gene: CSNK2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 619014
ClinVar RCV Id: RCV000757921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349699.1:p.Asp156His
CA407933108
NM_001362770.2:c.466G>C