Canonical Allele Identifier: PA2825276598
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230067

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Ser53Cys
CA10168065
NM_001005735.2:c.158C>G