Allele Registry

Canonical Allele Identifier: PA287266

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000115379

RCV000546737

RCV000575160

RCV003997235

ClinVar Variation:

127561

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Ser549Tyr	CA008999 NM_000179.3:c.1646C>A