Allele Registry

Canonical Allele Identifier: PA2827321551

Gene: RPGRIP1L HGNC NCBI

ClinVar RCV:

RCV000001126

ClinVar Variation:

1071

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317467.1:p.Ala695Pro	CA251694 NM_001330538.2:c.2083G>C