Canonical Allele Identifier: PA2825276601
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1003619
ClinVar RCV Id: RCV001300193
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Ser53Ala
CA411090974
NM_001005735.2:c.157T>G