Canonical Allele Identifier: PA2828227708
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 9898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354180.1:p.Pro235Ser
CA226435
NM_001367251.1:c.703C>T