Canonical Allele Identifier: PA211676
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 161300
ClinVar RCV Id: RCV000148638 RCV000411526 RCV000491584 RCV000471467 RCV000588732 RCV001175338 RCV004532667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile735Val
CA020218
NM_000251.3:c.2203A>G