Canonical Allele Identifier: PA2826445270
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244316.1:p.Leu291Val
CA166627
NM_001257387.2:c.871C>G