Allele Registry

Canonical Allele Identifier: PA104656

Gene: RHO HGNC NCBI

ClinVar Allele:

152799

ClinVar RCV:

RCV000132600

RCV001384606

RCV003888544

ClinVar Variation:

143081

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Gly188Arg	CA270025 NM_000539.3:c.562G>A CA354499264 NM_000539.3:c.562G>C