Allele Registry

Canonical Allele Identifier: PA104840

Gene: RHO HGNC NCBI

ClinVar Variation Id: 13019

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Phe45Leu	CA256666 NM_000539.3:c.133T>C CA354495891 NM_000539.3:c.135T>A CA354495894 NM_000539.3:c.135T>G