Canonical Allele Identifier: PA2826463944
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237362
ClinVar RCV Id: RCV001185296 RCV001319460 RCV003469136
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln343Glu
CA10582010
NM_001258281.1:c.1027C>G