Allele Registry

Canonical Allele Identifier: PA1139671454

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV001093177

ClinVar Variation:

872602

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Asn15Ile	CA354495329 NM_000539.3:c.44A>T