Allele Registry

Canonical Allele Identifier: PA2826586933

Gene: MSH6 HGNC NCBI

ClinVar Variation Id: 483785

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Glu1008Lys	CA346761475 NM_001281494.2:c.3022G>A