Canonical Allele Identifier: PA190237
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 184848
ClinVar RCV Id: RCV000164175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009125.1:p.Leu309Gln
CA190236
NM_007194.4:c.926T>A