Canonical Allele Identifier: PA2828064835
Gene: CSNK2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 432689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349700.1:p.Tyr50Cys
CA407940083
NM_001362771.2:c.149A>G