Allele Registry

Canonical Allele Identifier: PA645383885

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV000442591

RCV003889887

ClinVar Variation:

381626

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Leu88Pro	CA16604468 NM_000539.3:c.263T>C