Canonical Allele Identifier: PA2830302838
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182439

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Pro455Thr
CA299090
NM_145862.2:c.1363C>A