Allele Registry

Canonical Allele Identifier: PA2826636832

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000165958

RCV000214010

RCV000473325

RCV001526922

RCV003468765

RCV003995466

ClinVar Variation:

186374

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Arg657Cys	CA011024 NM_001281494.2:c.1969C>T