Canonical Allele Identifier: PA2579918639
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230819
ClinVar RCV Id: RCV004522933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Tyr588His
CA346728253
NM_000251.3:c.1762T>C