Canonical Allele Identifier: PA2828731773
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2068787
ClinVar RCV Id: RCV002975096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364877.1:p.Glu338Ala
CA388867889
NM_001377948.1:c.1013A>C