Allele Registry

Canonical Allele Identifier: PA104920

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV000013909

RCV001003172

RCV001582479

ClinVar Variation:

13034

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Pro267Leu	CA256680 NM_000539.3:c.800C>T