Canonical Allele Identifier: PA2826463606
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 450154
ClinVar RCV Id: RCV000521057 RCV002384007 RCV003449485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Cys267Trp
CA346733125
NM_001258281.1:c.801T>G