Canonical Allele Identifier: PA2825276690
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 234069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Pro80Ser
CA10168056
NM_001005735.2:c.238C>T