Canonical Allele Identifier: PA2826465828
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135859
ClinVar RCV Id: RCV000122987 RCV000411448 RCV000563636 RCV003149838 RCV002469017 RCV003997407
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys806Arg
CA020814
NM_001258281.1:c.2417A>G