Canonical Allele Identifier: PA2579921990
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2036400
ClinVar RCV Id: RCV002881945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala789Asp
CA346730034
NM_000251.3:c.2366C>A