Canonical Allele Identifier: PA645502591
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 403388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030025.1:p.Val1144Ile
CA10385143
NM_001034853.2:c.3430G>A