Allele Registry

Canonical Allele Identifier: PA2826636974

Gene: MSH6 HGNC NCBI

ClinVar Allele:

232794

ClinVar RCV:

RCV000222273

RCV000464929

RCV000478635

RCV003469091

RCV003998590

ClinVar Variation:

233992

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Glu690Lys	CA069899 NM_001281494.2:c.2068G>A