Canonical Allele Identifier: PA2825277192
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 957042
ClinVar RCV Id: RCV001229953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Lys355Thr
CA411100012
NM_001005735.2:c.1064A>C