Canonical Allele Identifier: PA2828223635
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 425491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354174.1:p.Leu100Pro
CA16621889
NM_001367245.1:c.299T>C