Canonical Allele Identifier: PA916077070
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 583047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Ile38Val
CA10168074
NM_145862.2:c.112A>G