Allele Registry

Canonical Allele Identifier: PA105066

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV000013929

ClinVar Variation:

13054

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Thr94Ile	CA122825 NM_000539.3:c.281C>T