Allele Registry

Canonical Allele Identifier: PA915984254

Gene: MSH2 HGNC NCBI

ClinVar RCV:

RCV000821319

RCV001022532

RCV001358250

RCV003452941

ClinVar Variation:

91099

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245210.1:p.Gly83Asp	CA021170 NM_001258281.1:c.248G>A