Allele Registry

Canonical Allele Identifier: PA645476040

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000460192

RCV000580161

RCV003317217

RCV004000789

ClinVar Variation:

408526

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.Ile865Thr	CA036766 NM_000251.3:c.2594T>C