Canonical Allele Identifier: PA227906
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99811
ClinVar RCV Id: RCV000086241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Asn569Lys
CA227905
NM_020366.4:c.1707T>G
CA388865928
NM_020366.4:c.1707T>A