Allele Registry

Canonical Allele Identifier: PA332427

Gene: MSH2 HGNC NCBI

MaveDb:

Score -4.4065153248

ClinVar RCV:

RCV000122984

RCV001013915

RCV001586659

RCV001882708

RCV003997406

ClinVar Variation:

135856

1213458

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Gln662His	CA019664 NM_000251.3:c.1986G>C CA346728893 NM_000251.3:c.1986G>T