Allele Registry

Canonical Allele Identifier: PA645484316

Gene: RTTN HGNC NCBI

ClinVar Variation Id: 327761

ClinVar Variation Id: 2703633

ClinVar RCV Id: RCV003579421

HGVS (amino-acid)	Matching Registered Transcripts
NP_775901.3:p.Gly242dup	CA8996378 NM_173630.3:c.725_727dup CA8996379 NM_173630.3:c.727_728insGGG CA8996380 NM_173630.3:c.725_726insGGG CA645607218 NM_173630.3:c.723_725dup CA991588204 NM_173630.3:c.727_728insGTG CA2642182857 NM_173630.3:c.725_726insCGG