Allele Registry

Canonical Allele Identifier: PA1139671520

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV001262654

ClinVar Variation:

982921

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Pro23Ser	CA354495494 NM_000539.3:c.67C>T