Allele Registry

Canonical Allele Identifier: PA2826465125

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000491777

RCV001356221

RCV003593972

ClinVar Variation:

428522

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Phe628Ser	CA346729201 NM_001258281.1:c.1883T>C