Canonical Allele Identifier: PA2579911352
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1373165
ClinVar RCV Id: RCV001880679 RCV002334780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val155Ile
CA346730527
NM_000251.3:c.463G>A