Allele Registry

Canonical Allele Identifier: PA094996

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000076546

RCV002433581

RCV002465507

ClinVar Variation:

91044

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Leu93Phe	CA020925 NM_000251.3:c.277C>T