Allele Registry

Canonical Allele Identifier: PA2826626188

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000115379

RCV000546737

RCV000575160

RCV003997235

ClinVar Variation:

127561

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ser419Tyr	CA008999 NM_001281492.2:c.1256C>A