Canonical Allele Identifier: PA2827476580
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182457

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Gly275Ser
CA299120
NM_001349956.2:c.823G>A