Canonical Allele Identifier: PA658673009
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455560
ClinVar RCV Id: RCV000553342 RCV000679305 RCV002456044 RCV004003745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn792Lys
CA346730082
NM_000251.3:c.2376T>A
CA346730085
NM_000251.3:c.2376T>G