Canonical Allele Identifier: PA2826465338
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483667
ClinVar RCV Id: RCV000561848 RCV001065224 RCV003987610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile681Val
CA346729739
NM_001258281.1:c.2041A>G