Canonical Allele Identifier: PA2826465747
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91003
ClinVar RCV Id: RCV000662430 RCV000692140 RCV000774582 RCV001818241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Tyr790Cys
CA020747
NM_001258281.1:c.2369A>G