Canonical Allele Identifier: PA2827474591
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 863628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Pro92Thr
CA411090430
NM_001349956.2:c.274C>A