Allele Registry

Canonical Allele Identifier: PA2826626133

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000131295

RCV000693545

RCV003998099

ClinVar Variation:

142272

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Ser406Asn	CA008866 NM_001281492.2:c.1217G>A