Canonical Allele Identifier: PA2826444738
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 142917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244316.1:p.Cys164Arg
CA169759
NM_001257387.2:c.490T>C