Canonical Allele Identifier: PA2826934425
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1378359
ClinVar RCV Id: RCV001881097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295263.1:p.Ile794Thr
CA395914741
NM_001308334.3:c.2381T>C