Allele Registry

Canonical Allele Identifier: PA104597

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV000013913

RCV000787679

RCV001074389

RCV001207877

RCV001229349

ClinVar Variation:

13038

956525

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Gly106Arg	CA256683 NM_000539.3:c.316G>A CA354496864 NM_000539.3:c.316G>C