Canonical Allele Identifier: PA2580140589
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 2070780
ClinVar RCV Id: RCV002971410

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030025.1:p.Ile1091Val
CA327914544
NM_001034853.2:c.3271A>G