Canonical Allele Identifier: PA645502580
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 257193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030025.1:p.Ala781Thr
CA10385291
NM_001034853.2:c.2341G>A