Allele Registry

Canonical Allele Identifier: PA1139671638

Gene: RHO HGNC NCBI

ClinVar Variation Id: 866607

ClinVar RCV Id: RCV001074739

ClinVar Variation Id: 1935435

ClinVar RCV Id: RCV002657777

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Ser93Arg	CA354496677 NM_000539.3:c.277A>C CA354496686 NM_000539.3:c.279C>A CA354496688 NM_000539.3:c.279C>G