Canonical Allele Identifier: PA2579913616
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1720466
ClinVar RCV Id: RCV002298201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu290Gln
CA346732874
NM_000251.3:c.868G>C