Canonical Allele Identifier: PA104505
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13040

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Asp190Tyr
CA256684
NM_000539.3:c.568G>T