Canonical Allele Identifier: PA2826465398
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408557
ClinVar RCV Id: RCV000456782 RCV002446814 RCV003449137
ClinVar Variation Id: 483671
ClinVar RCV Id: RCV000564777 RCV001844200 RCV001858296 RCV003451247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly695Arg
CA16610823
NM_001258281.1:c.2083G>A
CA346729821
NM_001258281.1:c.2083G>C