Allele Registry

Canonical Allele Identifier: PA2825092103

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002348927

ClinVar Variation:

1734099

HGVS (amino-acid)	Matching Registered Transcripts
NP_000170.1:p.Glu1234dup	CA2580067290 NM_000179.3:c.3700_3702dup