Canonical Allele Identifier: PA2830301014
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 140932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Ser252Asn
CA163957
NM_145862.2:c.755G>A