Canonical Allele Identifier: PA2827474172
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 803659
ClinVar RCV Id: RCV000990398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Ser40Gly
CA411091348
NM_001349956.2:c.118A>G