Allele Registry

Canonical Allele Identifier: PA104722

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV001090664

ClinVar Variation:

870954

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.His211Arg	CA354469894 NM_000539.3:c.632A>G