Canonical Allele Identifier: PA2827476329
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142376

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Lys250Glu
CA168192
NM_001349956.2:c.748A>G