Canonical Allele Identifier: PA2499286021
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1020461
ClinVar RCV Id: RCV001320041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Tyr659Ser
CA388867424
NM_020366.4:c.1976A>C