Canonical Allele Identifier: PA2830301625
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 420003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Thr323Pro
CA16621062
NM_145862.2:c.967A>C