Canonical Allele Identifier: PA2499286022
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1026037
ClinVar RCV Id: RCV001326438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.His664Arg
CA7089135
NM_020366.4:c.1991A>G