Canonical Allele Identifier: PA299102
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Ser57Phe
CA299101
NM_007194.4:c.170C>T