Canonical Allele Identifier: PA299341
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182571
ClinVar RCV Id: RCV000160602 RCV000410402 RCV000491763 RCV000761096 RCV001085231 RCV001193853 RCV001354130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Cys707Tyr
CA020070
NM_000251.3:c.2120G>A