Canonical Allele Identifier: PA645509907
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 439186
ClinVar RCV Id: RCV000507809 RCV000541857 RCV000572189 RCV000986669 RCV004003546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg444His
CA346724650
NM_000251.3:c.1331G>A