Canonical Allele Identifier: PA2828223816
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 9898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354174.1:p.Pro234Ser
CA226435
NM_001367245.1:c.700C>T