Allele Registry

Canonical Allele Identifier: PA2499233095

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV001304240

ClinVar Variation:

1007101

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Ala153Asp	CA354498362 NM_000539.3:c.458C>A