Canonical Allele Identifier: PA229176
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 100874

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Asp660Tyr
CA229175
NM_020366.4:c.1978G>T