Canonical Allele Identifier: PA2828227740
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 9899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354180.1:p.Gly275Ser
CA226447
NM_001367251.1:c.823G>A