Allele Registry

Canonical Allele Identifier: PA2826465417

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000484269

RCV000527665

RCV000563540

RCV003464020

RCV004003352

ClinVar Variation:

421405

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Ile700Met	CA16617601 NM_001258281.1:c.2100A>G