Allele Registry

Canonical Allele Identifier: PA2579914510

Gene: MSH2 HGNC NCBI

MaveDb:

Score -3.8223544062

ClinVar RCV:

RCV002383674

ClinVar Variation:

1771017

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln344Glu	CA346733185 NM_000251.3:c.1030C>G