Canonical Allele Identifier: PA2828226202
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 9916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354178.1:p.Gly172Arg
CA120805
NM_001367249.1:c.514G>C