Canonical Allele Identifier: PA916077073
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 410024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Ser39Pro
CA16616578
NM_145862.2:c.115T>C