Canonical Allele Identifier: PA2579910347
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1797805
ClinVar RCV Id: RCV002440055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Tyr98Asp
CA346729611
NM_000251.3:c.292T>G