Canonical Allele Identifier: PA299083
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182435
ClinVar RCV Id: RCV000160434 RCV000576132 RCV000704401 RCV000764374
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Pro393Leu
CA299082
NM_007194.4:c.1178C>T