Canonical Allele Identifier: PA270039
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 143094
ClinVar RCV Id: RCV000132614
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030025.1:p.Ala308Pro
CA270037
NM_001034853.2:c.922G>C