Canonical Allele Identifier: PA2828731793
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364877.1:p.Gly388Glu
CA227910
NM_001377948.1:c.1163G>A