Canonical Allele Identifier: PA2580443734
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2068787
ClinVar RCV Id: RCV002975096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Glu696Ala
CA388867889
NM_020366.4:c.2087A>C