Canonical Allele Identifier: PA2827476375
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 420003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Thr256Pro
CA16621062
NM_001349956.2:c.766A>C