Canonical Allele Identifier: PA168178
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142368

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Arg523Gly
CA168177
NM_007194.4:c.1567C>G