Canonical Allele Identifier: PA2827260993
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 319670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001315351.1:p.Leu57Phe
CA8058197
NM_001328422.2:c.171G>T
CA395925933
NM_001328422.2:c.171G>C