Canonical Allele Identifier: PA2826464688
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1780103
ClinVar RCV Id: RCV002404162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn530_Val532delinsThrSer
CA2580066948
NM_001258281.1:c.1589_1595delinsCATC