Canonical Allele Identifier: PA2827322112
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 241026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317467.1:p.Val1154Met
CA8057257
NM_001330538.2:c.3460G>A