Canonical Allele Identifier: PA2826465528
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 821205
ClinVar RCV Id: RCV001015390 RCV001799022 RCV002550805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn733del
CA645514884
NM_001258281.1:c.2197_2199del