Canonical Allele Identifier: PA2827321709
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 937727
ClinVar RCV Id: RCV001206809 RCV001833818 RCV002504241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317467.1:p.His825Arg
CA8057536
NM_001330538.2:c.2474A>G