Canonical Allele Identifier: PA2828227673
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 9916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354180.1:p.Gly173Arg
CA120805
NM_001367251.1:c.517G>C