Allele Registry

Canonical Allele Identifier: PA658673025

Gene: MSH2 HGNC NCBI

MaveDb:

Score -2.4884536058

ClinVar RCV:

RCV000566106

RCV001224509

ClinVar Variation:

483746

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.His801Leu	CA346730193 NM_000251.3:c.2402A>T