Canonical Allele Identifier: PA331519
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90982
ClinVar RCV Id: RCV001314549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln824Glu
CA020631
NM_000251.3:c.2470C>G