Canonical Allele Identifier: PA220677
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 92858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000319.1:p.Gly269Glu
CA220676
NM_000328.3:c.806G>A