Canonical Allele Identifier: PA2579910513
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1383519
ClinVar RCV Id: RCV001892658
ClinVar Variation Id: 2773595
ClinVar RCV Id: RCV003584451
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly108Arg
CA346729701
NM_000251.3:c.322G>A
CA346729709
NM_000251.3:c.322G>C