Allele Registry

Canonical Allele Identifier: PA2826629138

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000165367

RCV000482477

RCV000630080

RCV001262375

RCV003995412

ClinVar Variation:

185867

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Tyr1168Cys	CA014634 NM_001281492.2:c.3503A>G