Canonical Allele Identifier: PA287468
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127653
ClinVar RCV Id: RCV000115543 RCV000629878 RCV001017743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser281Pro
CA022412
NM_000251.3:c.841T>C