Canonical Allele Identifier: PA2830303079
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Ser476Thr
CA299094
NM_145862.2:c.1426T>A