Canonical Allele Identifier: PA2826934705
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 241026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295263.1:p.Val1142Met
CA8057257
NM_001308334.3:c.3424G>A