Canonical Allele Identifier: PA294016
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 140959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Met381Val
CA294015
NM_007194.4:c.1141A>G