Allele Registry

Canonical Allele Identifier: PA170858

Gene: RPGRIP1 HGNC NCBI

ClinVar RCV:

RCV000144462

ClinVar Variation:

156380

HGVS (amino-acid)	Matching Registered Transcripts
NP_065099.3:p.His631Leu	CA170857 NM_020366.4:c.1892A>T