Canonical Allele Identifier: PA2827476599
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 232564
ClinVar RCV Id: RCV000214665 RCV000759771 RCV000807751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Ile277Met
CA10167741
NM_001349956.2:c.831A>G