Allele Registry

Canonical Allele Identifier: PA2826628615

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV001971716

RCV002458921

ClinVar Variation:

1477689

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Glu1063Ala	CA346760508 NM_001281492.2:c.3188A>C