Allele Registry

Canonical Allele Identifier: PA2826464976

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000629738

RCV001179138

RCV004002773

ClinVar Variation:

525622

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Lys595Glu	CA346728873 NM_001258281.1:c.1783A>G