Allele Registry

Canonical Allele Identifier: PA299381

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000203841

RCV000565478

RCV000708846

RCV000759828

RCV001193897

RCV001354344

RCV003467250

ClinVar Variation:

182587

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ala869Glu	CA020801 NM_000251.3:c.2606C>A