Allele Registry

Canonical Allele Identifier: PA2826463545

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000168245

RCV001019487

RCV003995617

ClinVar Variation:

188267

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Asp253Val	CA022616 NM_001258281.1:c.758A>T