Allele Registry

Canonical Allele Identifier: PA256692

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV000013926

RCV001386999

ClinVar Variation:

13051

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Cys264del	CA256691 NM_000539.3:c.792_794del