Canonical Allele Identifier: PA658800409
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 501957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000319.1:p.Asp382Val
CA10385532
NM_000328.3:c.1145A>T