Allele Registry

Canonical Allele Identifier: PA2826465869

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000221700

RCV000524618

ClinVar Variation:

233504

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Glu815Gln	CA10578013 NM_001258281.1:c.2443G>C