Canonical Allele Identifier: PA2580443732
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2038619
ClinVar RCV Id: RCV002907666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Gln695Arg
CA7089149
NM_020366.4:c.2084A>G