Canonical Allele Identifier: PA2826462828
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1796436
ClinVar RCV Id: RCV002441810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu28Pro
CA346729590
NM_001258281.1:c.83T>C