Canonical Allele Identifier: PA2825276600
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1519805
ClinVar RCV Id: RCV002043789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005735.1:p.Ser53Phe
CA411090965
NM_001005735.2:c.158C>T