Canonical Allele Identifier: PA2826466050
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1796064
ClinVar RCV Id: RCV002441438
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys865Ile
CA346732242
NM_001258281.1:c.2594A>T