Allele Registry

Canonical Allele Identifier: PA104443

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV001946834

ClinVar Variation:

1456261

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Arg135Gly	CA354498053 NM_000539.3:c.403C>G