Allele Registry

Canonical Allele Identifier: PA2826634784

Gene: MSH6 HGNC NCBI

ClinVar Variation Id: 216297

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Glu182Lys	CA338881 NM_001281494.2:c.544G>A