Canonical Allele Identifier: PA645418331
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 285108
ClinVar RCV Id: RCV000276671 RCV000322396 RCV000358467 RCV000959229 RCV003940004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Ala181Gly
CA7088688
NM_020366.4:c.542C>G