Canonical Allele Identifier: PA226436
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 9898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000319.1:p.Pro235Ser
CA226435
NM_000328.3:c.703C>T