Allele Registry

Canonical Allele Identifier: PA2828731728

Gene: RPGRIP1 HGNC NCBI

ClinVar RCV:

RCV000144462

ClinVar Variation:

156380

HGVS (amino-acid)	Matching Registered Transcripts
NP_001364877.1:p.His273Leu	CA170857 NM_001377948.1:c.818A>T