Allele Registry

Canonical Allele Identifier: PA2826628805

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002348936

ClinVar Variation:

1734109

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Leu1105_Glu1107del	CA2580067291 NM_001281492.2:c.3312_3320del