Canonical Allele Identifier: PA916077113
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 410069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_665861.1:p.Ser55Phe
CA10168064
NM_145862.2:c.164C>T