Canonical Allele Identifier: PA2499286000
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1061631
ClinVar RCV Id: RCV001371248
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Arg118His
CA7088640
NM_020366.4:c.353G>A