Canonical Allele Identifier: PA916046286
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 9899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354177.1:p.Gly285Ser
CA226447
NM_001367248.1:c.853G>A