Canonical Allele Identifier: PA2580140602
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 2051629
ClinVar RCV Id: RCV002927400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030025.1:p.Ser1126Leu
CA412726735
NM_001034853.2:c.3377C>T