Allele Registry

Canonical Allele Identifier: PA2826463829

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000214618

RCV000409794

RCV000480571

RCV000546544

RCV000761006

RCV003387810

ClinVar Variation:

232371

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Arg316Cys	CA027079 NM_001258281.1:c.946C>T