Allele Registry

Canonical Allele Identifier: PA2826463806

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV001038694

ClinVar Variation:

837376

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln311Glu	CA027045 NM_001258281.1:c.931C>G