Allele Registry

Canonical Allele Identifier: PA336688

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000196756

RCV000214843

RCV000409612

RCV000586261

RCV003997013

ClinVar Variation:

216342

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Arg444Leu	CA027957 NM_000251.3:c.1331G>T