Canonical Allele Identifier: PA916077110
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 133888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Ser53Thr
CA158095
NM_145862.2:c.157T>A