Canonical Allele Identifier: PA094788
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90883
ClinVar RCV Id: RCV000076385 RCV000571689 RCV003593899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Cys697Phe
CA019999
NM_000251.3:c.2090G>T