Allele Registry

Canonical Allele Identifier: PA645470939

Gene: MSH2 HGNC NCBI

MaveDb:

Score -5.1005279397

ClinVar RCV:

RCV000235367

RCV000572196

RCV000688689

RCV003463696

ClinVar Variation:

245828

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ser13Asn	CA10584201 NM_000251.3:c.38G>A