Allele Registry

Canonical Allele Identifier: PA2826637767

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV002348927

ClinVar Variation:

1734099

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268423.1:p.Glu932dup	CA2580067290 NM_001281494.2:c.2794_2796dup