Allele Registry

Canonical Allele Identifier: PA2741816667

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV003725880

ClinVar Variation:

2894558

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Glu150Asp	CA354498294 NM_000539.3:c.450G>C CA354498295 NM_000539.3:c.450G>T