Canonical Allele Identifier: PA2827321550
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1965869
ClinVar RCV Id: RCV002711429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317467.1:p.Ala695Lys
CA2580091682
NM_001330538.2:c.2083_2084delinsAA