Canonical Allele Identifier: PA071659
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 221937
ClinVar RCV Id: RCV000207372 RCV000384797 RCV001002218 RCV001800533 RCV001086986 RCV001800534 RCV003955239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Ile270Val
CA071653
NM_020366.4:c.808A>G