Canonical Allele Identifier: PA2826933998
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1366056
ClinVar RCV Id: RCV001961959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295263.1:p.Arg251Pro
CA395923780
NM_001308334.3:c.752G>C