Canonical Allele Identifier: PA2827474216
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 631296

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Ser44Thr
CA411091212
NM_001349956.2:c.131G>C