Canonical Allele Identifier: PA331562
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91047
ClinVar RCV Id: RCV000411744 RCV000691322 RCV001016615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile930Met
CA020945
NM_000251.3:c.2790A>G