Canonical Allele Identifier: PA2826445060
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 232039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244316.1:p.Leu239Val
CA10581033
NM_001257387.2:c.715C>G