Canonical Allele Identifier: PA2829355717
Gene: CSNK2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 432689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001886.1:p.Tyr50Cys
CA407940083
NM_001895.4:c.149A>G