Canonical Allele Identifier: PA2826464782
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 960712
ClinVar RCV Id: RCV001234287 RCV002411866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly548Glu
CA346728398
NM_001258281.1:c.1643G>A