Canonical Allele Identifier: PA2579912736
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230853
ClinVar RCV Id: RCV004522967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile237Phe
CA346732051
NM_000251.3:c.709A>T