Allele Registry

Canonical Allele Identifier: PA1139672186

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV001265162

ClinVar Variation:

984768

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Lys296Gln	CA354470787 NM_000539.3:c.886A>C