Canonical Allele Identifier: PA916046259
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 98784

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354177.1:p.Arg137Gly
CA226416
NM_001367248.1:c.409A>G