Canonical Allele Identifier: PA2827474141
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230039
ClinVar RCV Id: RCV000220647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Gly37Asp
CA10581113
NM_001349956.2:c.110G>A