Canonical Allele Identifier: PA2826466042
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127639
ClinVar RCV Id: RCV000583830 RCV000759829 RCV000469769 RCV003997275 RCV000662933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg863Gln
CA020939
NM_001258281.1:c.2588G>A