Allele Registry

Canonical Allele Identifier: PA2826464760

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000428720

RCV000663086

RCV000707667

RCV001526105

ClinVar Variation:

90797

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.His544Asn	CA019403 NM_001258281.1:c.1630C>A