Canonical Allele Identifier: PA2826463055
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91147
ClinVar RCV Id: RCV000160619 RCV002354269 RCV003452954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Cys133Tyr
CA021530
NM_001258281.1:c.398G>A