Allele Registry

Canonical Allele Identifier: PA2826464488

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000411811

RCV000506572

RCV000697749

RCV001191249

RCV001800374

ClinVar Variation:

90713

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Asn481Ser	CA018784 NM_001258281.1:c.1442A>G