Canonical Allele Identifier: PA104680
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13047
ClinVar RCV Id: RCV000013922 RCV001237838 RCV003390680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Gly51Arg
CA256687
NM_000539.3:c.151G>C