Canonical Allele Identifier: PA2580443704
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2116829
ClinVar RCV Id: RCV003027434

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Thr652Ala
CA388867351
NM_020366.4:c.1954A>G