Canonical Allele Identifier: PA2826445248
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244316.1:p.Ser284Thr
CA299094
NM_001257387.2:c.850T>A