Canonical Allele Identifier: PA916046258
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 425491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354177.1:p.Leu110Pro
CA16621889
NM_001367248.1:c.329T>C