Canonical Allele Identifier: PA2828064862
Gene: CSNK2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1033457
ClinVar RCV Id: RCV001335876

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349700.1:p.Asn161Asp
CA407933000
NM_001362771.2:c.481A>G