Canonical Allele Identifier: PA2825276558
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 803659
ClinVar RCV Id: RCV000990398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Ser40Gly
CA411091348
NM_001005735.2:c.118A>G