Canonical Allele Identifier: PA2825276599
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 133888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Ser53Thr
CA158095
NM_001005735.2:c.157T>A