Canonical Allele Identifier: PA2827322139
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 965972
ClinVar RCV Id: RCV001240541 RCV001586080 RCV001828953 RCV002480797 RCV002563977 RCV004538500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317467.1:p.Ile1186Val
CA8057226
NM_001330538.2:c.3556A>G