Canonical Allele Identifier: PA226419
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 9897
ClinVar RCV Id: RCV000010575 RCV000085105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000319.1:p.Phe130Cys
CA226418
NM_000328.3:c.389T>G