Canonical Allele Identifier: PA2827474398
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 966564
ClinVar RCV Id: RCV001241281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Ser73Pro
CA411090735
NM_001349956.2:c.217T>C