Canonical Allele Identifier: PA2828226327
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 9899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354178.1:p.Gly274Ser
CA226447
NM_001367249.1:c.820G>A