Canonical Allele Identifier: PA2826463603
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91272
ClinVar RCV Id: RCV000076777 RCV000491354 RCV002280101 RCV003452982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Cys267Arg
CA022717
NM_001258281.1:c.799T>C