Canonical Allele Identifier: PA2827474282
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 410069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Ser55Phe
CA10168064
NM_001349956.2:c.164C>T