Canonical Allele Identifier: PA2579922190
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773619
ClinVar RCV Id: RCV003584475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.His801Gln
CA346730194
NM_000251.3:c.2403T>A
CA346730195
NM_000251.3:c.2403T>G