Canonical Allele Identifier: PA228929
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 100589
ClinVar RCV Id: RCV000086972 RCV001059148 RCV001111368 RCV001111369 RCV002281926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Ile1120Val
CA228928
NM_020366.4:c.3358A>G