Allele Registry

Canonical Allele Identifier: PA658672404

Gene: MSH2 HGNC NCBI

MaveDb:

Score -4.5085531226

ClinVar RCV:

RCV000557128

RCV000570076

RCV001798872

RCV003459175

ClinVar Variation:

455487

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Asn465Ser	CA346726685 NM_000251.3:c.1394A>G