Canonical Allele Identifier: PA916077116
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Ser57Phe
CA299101
NM_145862.2:c.170C>T