Canonical Allele Identifier: PA227914
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99816
ClinVar RCV Id: RCV000086247 RCV000327868 RCV001081118 RCV001112991 RCV001112992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Arg86Trp
CA227913
NM_020366.4:c.256C>T