Allele Registry

Canonical Allele Identifier: PA2825092101

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002348936

ClinVar Variation:

1734109

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Leu1235_Glu1237del	CA2580067291 NM_000179.3:c.3702_3710del