Allele Registry

Canonical Allele Identifier: PA2826465797

Gene: MSH2 HGNC NCBI

ClinVar Allele:

392841

ClinVar RCV:

RCV000460192

RCV000580161

RCV003317217

RCV004000789

ClinVar Variation:

408526

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ile799Thr	CA036766 NM_001258281.1:c.2396T>C