Allele Registry

Canonical Allele Identifier: PA2826634719

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000074653

RCV000166488

RCV000222213

RCV000524109

RCV000587141

RCV001535649

RCV003450925

RCV004528269

ClinVar Variation:

89191

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Arg166Cys	CA008576 NM_001281494.2:c.496C>T