Canonical Allele Identifier: PA2827478600
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141856
ClinVar RCV Id: RCV000130543 RCV000197078 RCV000587712 RCV000764367
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336885.1:p.Leu445Val
CA166627
NM_001349956.2:c.1333C>G