Canonical Allele Identifier: PA2826934310
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1080
ClinVar RCV Id: RCV000001135 RCV000201757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295263.1:p.Ser659Pro
CA210651
NM_001308334.3:c.1975T>C