Allele Registry

Canonical Allele Identifier: PA186769

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000162700

RCV000213163

RCV000411429

RCV000627690

RCV001255541

RCV003460658

RCV003997063

ClinVar Variation:

89176

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.His382Tyr	CA008133 NM_000179.3:c.1144C>T