Allele Registry

Canonical Allele Identifier: PA2826465227

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000206475

RCV001181937

RCV003230453

RCV003468962

ClinVar Variation:

220779

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ser651Asn	CA034373 NM_001258281.1:c.1952G>A