Allele Registry

Canonical Allele Identifier: PA2826626795

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000074709

RCV000128865

RCV000212657

RCV000524130

RCV000576301

RCV000583928

RCV001353773

RCV001526863

ClinVar Variation:

89245

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gly556Asp	CA009620 NM_001281492.2:c.1667G>A