Canonical Allele Identifier: PA2826465628
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90982
ClinVar RCV Id: RCV001314549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln758Glu
CA020631
NM_001258281.1:c.2272C>G