Canonical Allele Identifier: PA2826444725
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 140959
ClinVar RCV Id: RCV000129242 RCV000227000 RCV000212452 RCV000764375 RCV001354869 RCV000781303
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244316.1:p.Met160Val
CA294015
NM_001257387.2:c.478A>G