Canonical Allele Identifier: PA2827321707
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1304261
ClinVar RCV Id: RCV001752028 RCV002488533 RCV002539919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317467.1:p.Ala823Leu
CA2573054237
NM_001330538.2:c.2467_2468delinsTT