Canonical Allele Identifier: PA2828226868
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 9902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354179.1:p.Gly60Val
CA226376
NM_001367250.1:c.179G>T