Canonical Allele Identifier: PA2826464393
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1759
ClinVar RCV Id: RCV000001829 RCV000076197 RCV000165648 RCV000256140 RCV000531855 RCV001251063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg458Pro
CA018643
NM_001258281.1:c.1373G>C