Canonical Allele Identifier: PA2828225032
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 438137
ClinVar RCV Id: RCV000504753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354176.1:p.Cys42Trp
CA412745785
NM_001367247.1:c.126T>G