Allele Registry

Canonical Allele Identifier: PA2826463861

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000167351

RCV000629828

RCV003329248

RCV003444210

ClinVar Variation:

187607

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Arg323Gln	CA017397 NM_001258281.1:c.968G>A