Allele Registry

Canonical Allele Identifier: PA2826627390

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000129131

RCV000226891

RCV001140447

RCV003997483

RCV004532546

ClinVar Variation:

140892

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Val698Ile	CA010298 NM_001281492.2:c.2092G>A