Allele Registry

Canonical Allele Identifier: PA658671655

Gene: MSH2 HGNC NCBI

MaveDb:

Score -2.2837006681

ClinVar Allele:

472770

ClinVar RCV:

RCV000563996

RCV001324767

RCV004001204

ClinVar Variation:

487004

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Asp133Gly	CA46677666 NM_000251.3:c.398A>G