Allele Registry

Canonical Allele Identifier: PA104980

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV000013912

RCV000504903

RCV002513029

ClinVar Variation:

13037

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Pro53Arg	CA256682 NM_000539.3:c.158C>G