Canonical Allele Identifier: PA226417
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 98784

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000319.1:p.Arg127Gly
CA226416
NM_000328.3:c.379A>G