Canonical Allele Identifier: PA2826465474
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141236
ClinVar RCV Id: RCV000129653 RCV001047553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.His717Arg
CA020486
NM_001258281.1:c.2150A>G