Canonical Allele Identifier: PA2827474038
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 229673
ClinVar Variation Id: 483400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Ser31_Gly37dup
CA10168075
NM_001349956.2:c.87_107dup
CA10581112
NM_001349956.2:c.91_111dup