Allele Registry

Canonical Allele Identifier: PA1139671773

Gene: RHO HGNC NCBI

ClinVar RCV:

RCV001203997

ClinVar Variation:

935409

HGVS (amino-acid)	Matching Registered Transcripts
NP_000530.1:p.Asn151Ser	CA354498309 NM_000539.3:c.452A>G