Allele Registry

Canonical Allele Identifier: PA293898

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000074709

RCV000128865

RCV000212657

RCV000524130

RCV000576301

RCV000583928

RCV001353773

RCV001526863

ClinVar Variation:

89245

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Gly686Asp	CA009620 NM_000179.3:c.2057G>A