Allele Registry

Canonical Allele Identifier: PA2573171416

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV002018102

ClinVar Variation:

1509710

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Ala153Val	CA354498363 NM_000539.3:c.458C>T