Canonical Allele Identifier: PA2826934386
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 166909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295263.1:p.Arg747Gln
CA233780
NM_001308334.3:c.2240G>A