Allele Registry

Canonical Allele Identifier: PA2826629203

Gene: MSH6 HGNC NCBI

ClinVar Variation Id: 483785

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Glu1180Lys	CA346761475 NM_001281492.2:c.3538G>A