Canonical Allele Identifier: PA916046268
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 9916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354177.1:p.Gly183Arg
CA120805
NM_001367248.1:c.547G>C