Allele Registry

Canonical Allele Identifier: PA104733

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV000013901

RCV001074697

ClinVar Variation:

13027

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.His211Pro	CA256674 NM_000539.3:c.632A>C