Canonical Allele Identifier: PA226377
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 9902
ClinVar RCV Id: RCV000010580 RCV000085072 RCV000822760 RCV001074755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000319.1:p.Gly60Val
CA226376
NM_000328.3:c.179G>T