Allele Registry

Canonical Allele Identifier: PA2826465562

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000205485

RCV000480146

RCV000568311

RCV000708843

ClinVar Variation:

219534

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Thr740Ile	CA035718 NM_001258281.1:c.2219C>T