Allele Registry

Canonical Allele Identifier: PA915984140

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000197978

RCV000217291

RCV000515278

RCV000590606

RCV000662843

RCV003330516

RCV003998481

ClinVar Variation:

182576

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Leu62Arg	CA021103 NM_001258281.1:c.185T>G