Canonical Allele Identifier: PA1139738550
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 834237
ClinVar RCV Id: RCV001034879 RCV001074229 RCV001800938 RCV001800939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.His631Arg
CA7089115
NM_020366.4:c.1892A>G