Allele Registry

Canonical Allele Identifier: PA163702

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000129031

RCV000195792

RCV000657020

RCV000662484

RCV001002443

RCV003460882

RCV003997472

ClinVar Variation:

140836

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Arg761Gly	CA009950 NM_000179.3:c.2281A>G