Allele Registry

Canonical Allele Identifier: PA2826464881

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV003759998

ClinVar Variation:

2784531

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.His573Asn	CA346728648 NM_001258281.1:c.1717C>A