Canonical Allele Identifier: PA2826444757
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1056503

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244316.1:p.Thr168Ile
CA411096833
NM_001257387.2:c.503C>T