Allele Registry

Canonical Allele Identifier: PA2579919481

Gene: MSH2 HGNC NCBI

MaveDb:

Score -4.2436507026

ClinVar RCV:

RCV003759998

ClinVar Variation:

2784531

HGVS (amino-acid)	Matching Registered Transcripts
NP_000242.1:p.His639Asn	CA346728648 NM_000251.3:c.1915C>A