Allele Registry

Canonical Allele Identifier: PA339318

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000200437

RCV000216489

RCV001577165

RCV003997021

ClinVar Variation:

216355

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Thr796Ile	CA339316 NM_000251.3:c.2387C>T