Canonical Allele Identifier: PA299106
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182447
ClinVar Variation Id: 460821
ClinVar RCV Id: RCV000538696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Trp93Arg
CA299105
NM_007194.4:c.277T>C
CA411090411
NM_007194.4:c.277T>A