Canonical Allele Identifier: PA2825662019
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1379230
ClinVar RCV Id: RCV001883663 RCV002482623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121369.1:p.Arg797Ile
CA281339426
NM_001127897.1:c.2390G>T