Allele Registry

Canonical Allele Identifier: PA2826625949

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002397057

ClinVar Variation:

1773483

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Glu363del	CA2580067595 NM_001281492.2:c.1088_1090del