Canonical Allele Identifier: PA104701
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 13021
ClinVar RCV Id: RCV000013895 RCV001003167 RCV001213959 RCV001813740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000530.1:p.Gly89Asp
CA256668
NM_000539.3:c.266G>A