Allele Registry

Canonical Allele Identifier: PA256696

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV000013930

ClinVar Variation:

13055

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Pro23Ala	CA256695 NM_000539.3:c.67C>G