Canonical Allele Identifier: PA916046276
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 9898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354177.1:p.Pro245Ser
CA226435
NM_001367248.1:c.733C>T