Allele Registry

Canonical Allele Identifier: PA1139671571

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV001242415

RCV001265174

ClinVar Variation:

967490

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Thr58Met	CA2607073 NM_000539.3:c.173C>T