Canonical Allele Identifier: PA2830300201
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Asp162Gly
CA165091
NM_145862.2:c.485A>G