Allele Registry

Canonical Allele Identifier: PA2826465204

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000807667

ClinVar Variation:

652165

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Arg645Gly	CA346729287 NM_001258281.1:c.1933C>G