Canonical Allele Identifier: PA2827474291
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 920665
ClinVar RCV Id: RCV001179521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Ser57Pro
CA411090923
NM_001349956.2:c.169T>C