Canonical Allele Identifier: PA916077118
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Thr59Lys
CA167221
NM_145862.2:c.176C>A