Allele Registry

Canonical Allele Identifier: PA2826463626

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000462262

RCV001016976

RCV001800676

ClinVar Variation:

408496

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gln271Glu	CA16611022 NM_001258281.1:c.811C>G