Canonical Allele Identifier: PA2499286023
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1297122
ClinVar RCV Id: RCV001724826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Pro674Ser
CA388867610
NM_020366.4:c.2020C>T