Canonical Allele Identifier: PA104792
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13030
ClinVar RCV Id: RCV000013905 RCV002513028
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Lys296Glu
CA256677
NM_000539.3:c.886A>G