Allele Registry

Canonical Allele Identifier: PA2826628803

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002875937

ClinVar Variation:

2023785

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Lys1103del	CA2580067289 NM_001281492.2:c.3307_3309del