Allele Registry

Canonical Allele Identifier: PA645383136

Gene: MSH6 HGNC NCBI

ClinVar Allele:

232794

ClinVar RCV:

RCV000222273

RCV000464929

RCV000478635

RCV003469091

RCV003998590

ClinVar Variation:

233992

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu992Lys	CA069899 NM_000179.3:c.2974G>A