Canonical Allele Identifier: PA104490
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13023

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Asp190Asn
CA256670
NM_000539.3:c.568G>A