Canonical Allele Identifier: PA2825276719
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2000155
ClinVar RCV Id: RCV002797319

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Pro90Arg
CA411090464
NM_001005735.2:c.269C>G