Allele Registry

Canonical Allele Identifier: PA2826628090

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000222273

RCV000464929

RCV000478635

RCV003469091

RCV003998590

ClinVar Variation:

233992

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Glu862Lys	CA069899 NM_001281492.2:c.2584G>A