Canonical Allele Identifier: PA2825276639
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 128068
ClinVar RCV Id: RCV000116009 RCV000210191 RCV000199067 RCV000212407 RCV001270935 RCV002265610 RCV003153376 RCV003338414 RCV004528806 RCV002465520 RCV001149533 RCV001356247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Glu64Lys
CA288298
NM_001005735.2:c.190G>A