Canonical Allele Identifier: PA094657
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90986
ClinVar RCV Id: RCV000076488 RCV000131725 RCV000679306 RCV000659884 RCV001084815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala834Thr
CA020643
NM_000251.3:c.2500G>A