Allele Registry

Canonical Allele Identifier: PA167111

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000130794

RCV000507463

RCV000679222

RCV001083193

RCV003460666

RCV003997070

ClinVar Variation:

89237

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ile669Thr	CA009545 NM_000179.3:c.2006T>C