Allele Registry

Canonical Allele Identifier: PA645474283

Gene: MSH2 HGNC NCBI

MaveDb:

Score -2.2916925799

ClinVar RCV:

RCV000232170

RCV000573477

RCV000589179

RCV003998754

ClinVar Variation:

237365

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ala434Val	CA027829 NM_000251.3:c.1301C>T