Allele Registry

Canonical Allele Identifier: PA2826628808

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000491347

RCV000502171

ClinVar Variation:

428304

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Glu1104_Leu1105dup	CA645369302 NM_001281492.2:c.3311_3316dup