Canonical Allele Identifier: PA2827321386
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 406249
ClinVar RCV Id: RCV000457593 RCV001092930 RCV001833576 RCV002480366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317467.1:p.Val591Ala
CA8057705
NM_001330538.2:c.1772T>C