Canonical Allele Identifier: PA2827474180
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 568672
ClinVar RCV Id: RCV000689101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Ser42Thr
CA411091307
NM_001349956.2:c.124T>A