Canonical Allele Identifier: PA294327
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90619
ClinVar RCV Id: RCV000131211 RCV000212578 RCV000409784 RCV000764419 RCV000524339 RCV000656872 RCV001262887 RCV004537289 RCV003330424
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Tyr43Cys
CA017905
NM_000251.3:c.128A>G