Canonical Allele Identifier: PA915953996
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 420003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Thr366Pro
CA16621062
NM_001005735.2:c.1096A>C