Allele Registry

Canonical Allele Identifier: PA2573165221

Gene: MSH2 HGNC NCBI

MaveDb:

Score -2.1853243074

ClinVar RCV:

RCV001889948

ClinVar Variation:

1377625

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gly880Ala	CA346731331 NM_000251.3:c.2639G>C