Canonical Allele Identifier: PA2825276713
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2427867
ClinVar RCV Id: RCV003116838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Thr89Pro
CA411090484
NM_001005735.2:c.265A>C