Canonical Allele Identifier: PA227927
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99824
ClinVar RCV Id: RCV000086255 RCV001305369 RCV002225082 RCV002265604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Glu1279del
CA227926
NM_020366.4:c.3835_3837del