Allele Registry

Canonical Allele Identifier: PA2826637104

Gene: MSH6 HGNC NCBI

ClinVar Allele:

180085

ClinVar RCV:

RCV000160686

RCV000212674

RCV000411475

RCV000475900

RCV000766283

RCV003998499

ClinVar Variation:

182640

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Arg722Gln	CA011493 NM_001281494.2:c.2165G>A