Canonical Allele Identifier: PA299361
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182580
ClinVar RCV Id: RCV000160612 RCV000212587 RCV000477198 RCV001002118 RCV003444208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val161Ile
CA021193
NM_000251.3:c.481G>A