Canonical Allele Identifier: PA916077032
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 229673
ClinVar Variation Id: 483400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Ser31_Gly37dup