Canonical Allele Identifier: PA226448
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 9899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000319.1:p.Gly275Ser
CA226447
NM_000328.3:c.823G>A