Canonical Allele Identifier: PA2826465389
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 41866
ClinVar RCV Id: RCV000034800 RCV000986685 RCV002444462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly693Glu
CA020397
NM_001258281.1:c.2078G>A