Canonical Allele Identifier: PA891844693
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 570030
ClinVar RCV Id: RCV000690793 RCV001015003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Tyr757Cys
CA346729799
NM_000251.3:c.2270A>G