Allele Registry

Canonical Allele Identifier: PA357280

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000203760

RCV000662969

RCV000771214

RCV001569238

RCV003997617

ClinVar Variation:

220154

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ile169Met	CA039056 NM_000251.3:c.507A>G