Canonical Allele Identifier: PA194134
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 186199
ClinVar RCV Id: RCV000165747 RCV000589676 RCV000693732 RCV003995449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg680Gly
CA019866
NM_000251.3:c.2038C>G