Canonical Allele Identifier: PA2499285991
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1005094
ClinVar RCV Id: RCV001301904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Gly29Ser
CA388857088
NM_020366.4:c.85G>A