Canonical Allele Identifier: PA2825662199
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 319651
ClinVar RCV Id: RCV000304399 RCV000334324 RCV000400874 RCV004021662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121369.1:p.Ser1026Phe
CA8057349
NM_001127897.1:c.3077C>T