Canonical Allele Identifier: PA1139689452
Gene: CHEK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 957042
ClinVar RCV Id: RCV001229953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244316.1:p.Lys91Thr
CA411100012
NM_001257387.2:c.272A>C