Canonical Allele Identifier: PA1139738554
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 883035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Ser688Leu
CA7089145
NM_020366.4:c.2063C>T