Canonical Allele Identifier: PA2827474711
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 186864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Asp101Tyr
CA196080
NM_001349956.2:c.301G>T