Canonical Allele Identifier: PA2825661604
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 461759
ClinVar RCV Id: RCV001334836 RCV001829574 RCV000550791 RCV004537945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121369.1:p.Thr256Ile
CA8058034
NM_001127897.1:c.767C>T