Canonical Allele Identifier: PA2829697878
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014270
ClinVar RCV Id: RCV001312981

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Ser42Cys
CA411091279
NM_007194.4:c.125C>G