Canonical Allele Identifier: PA915957852
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 624396
ClinVar RCV Id: RCV000762618

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030025.1:p.Lys1138Arg
CA412726354
NM_001034853.2:c.3413A>G