Allele Registry

Canonical Allele Identifier: PA2826625400

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000132064

RCV000230863

RCV000589862

RCV000758606

RCV001420719

ClinVar Variation:

142698

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Arg231Cys	CA007972 NM_001281492.2:c.691C>T