Allele Registry

Canonical Allele Identifier: PA2826626516

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000219912

RCV000233003

RCV000484834

RCV000657004

RCV000662524

RCV003469017

RCV003997865

ClinVar Variation:

230869

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Gly494Ser	CA10578081 NM_001281492.2:c.1480G>A