Canonical Allele Identifier: PA891844702
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 580478
ClinVar RCV Id: RCV000704029 RCV001797134 RCV002442526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala791Val
CA346730067
NM_000251.3:c.2372C>T