Allele Registry

Canonical Allele Identifier: PA2826934342

Gene: RPGRIP1L HGNC NCBI

ClinVar RCV:

RCV000001126

ClinVar Variation:

1071

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295263.1:p.Ala695Pro	CA251694 NM_001308334.3:c.2083G>C