Allele Registry

Canonical Allele Identifier: PA357698

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000206475

RCV001181937

RCV003230453

RCV003468962

ClinVar Variation:

220779

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ser717Asn	CA034373 NM_000251.3:c.2150G>A