Canonical Allele Identifier: PA2827474273
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1003619
ClinVar RCV Id: RCV001300193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Ser53Ala
CA411090974
NM_001349956.2:c.157T>G