Allele Registry

Canonical Allele Identifier: PA331646

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000076652

RCV000811653

RCV002354270

ClinVar Variation:

91148

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Val200Asp	CA021536 NM_000251.3:c.599T>A