Allele Registry

Canonical Allele Identifier: PA658739528

Gene: MSH2 HGNC NCBI

MaveDb:

Score -2.4791461706

ClinVar RCV:

RCV000580076

RCV001236705

RCV003061533

RCV003465291

ClinVar Variation:

489937

2151932

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Thr812Ser	CA346730268 NM_000251.3:c.2434A>T CA346730271 NM_000251.3:c.2435C>G