Canonical Allele Identifier: PA2499230061
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1001399
ClinVar RCV Id: RCV001297688 RCV004036079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe276Ile
CA346732790
NM_000251.3:c.826T>A