Canonical Allele Identifier: PA2827474319
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1692943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Ser62Pro
CA411090862
NM_001349956.2:c.184T>C