Canonical Allele Identifier: PA1139740162
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_056087.2:p.His825Arg
CA8057536
NM_015272.2:c.2474A>G