Canonical Allele Identifier: PA165630
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141500
ClinVar RCV Id: RCV000130057 RCV000196356 RCV000202282 RCV000679311 RCV001355466 RCV001798439 RCV003997545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly137Arg
CA021142
NM_000251.3:c.409G>C