Allele Registry

Canonical Allele Identifier: PA094667

Gene: MSH2 HGNC NCBI

MaveDb:

Score 2.4903031569

ClinVar RCV:

RCV000076034

RCV001230748

RCV002415553

ClinVar Variation:

90539

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Arg359Ser	CA017208 NM_000251.3:c.1077A>T CA346733519 NM_000251.3:c.1077A>C