Canonical Allele Identifier: PA2826934348
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1370352
ClinVar RCV Id: RCV001870979 RCV004536393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295263.1:p.Glu702Gly
CA8057639
NM_001308334.3:c.2105A>G