Canonical Allele Identifier: PA2826463280
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237406
ClinVar RCV Id: RCV000234549 RCV000519279 RCV000766744 RCV001026663 RCV003998765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ser189Asn
CA040340
NM_001258281.1:c.566G>A