Canonical Allele Identifier: PA104526
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Cys110Tyr
CA256681
NM_000539.3:c.329G>A