Canonical Allele Identifier: PA2826444638
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1786420
ClinVar RCV Id: RCV002417797
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244316.1:p.Glu139Asp
CA411097510
NM_001257387.2:c.417G>T
CA411097517
NM_001257387.2:c.417G>C