Canonical Allele Identifier: PA916077081
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 631296

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Ser44Thr
CA411091212
NM_145862.2:c.131G>C