Canonical Allele Identifier: PA104415
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Ala164Glu
CA256689
NM_000539.3:c.491C>A