Canonical Allele Identifier: PA2830301878
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 140959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Met352Val
CA294015
NM_145862.2:c.1054A>G