Canonical Allele Identifier: PA226408
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 9906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000319.1:p.Thr99Asn
CA226407
NM_000328.3:c.296C>A