Allele Registry

Canonical Allele Identifier: PA163858

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000129131

RCV000226891

RCV001140447

RCV003997483

RCV004532546

ClinVar Variation:

140892

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Val828Ile	CA010298 NM_000179.3:c.2482G>A