Allele Registry

Canonical Allele Identifier: PA658672329

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000570734

RCV002528137

RCV004001039

ClinVar Variation:

483719

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.His428Asp	CA346724494 NM_000251.3:c.1282C>G