Canonical Allele Identifier: PA2827321551
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1071
ClinVar RCV Id: RCV000001126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317467.1:p.Ala695Pro
CA251694
NM_001330538.2:c.2083G>C