Canonical Allele Identifier: PA2579919156
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1961644
ClinVar RCV Id: RCV002720831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val620Ile
CA346728452
NM_000251.3:c.1858G>A