Canonical Allele Identifier: PA2825276556
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 410002
ClinVar RCV Id: RCV000463217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Ser40Thr
CA16616355
NM_001005735.2:c.119G>C