Canonical Allele Identifier: PA2573074578
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 100589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364877.1:p.Ile762Val
CA228928
NM_001377948.1:c.2284A>G