Allele Registry

Canonical Allele Identifier: PA165183

Gene: MSH2 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000129838

RCV000168339

RCV000482932

RCV000777250

RCV000807280

RCV001175571

RCV001352102

RCV001356219

RCV003335115

RCV003336181

RCV003997529

RCV004532554

ClinVar Variation:

141351

631127

1047398

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Met813Ile	CA020596 NM_000251.3:c.2439G>A CA46705323 NM_000251.3:c.2439G>C CA346730278 NM_000251.3:c.2439G>T