Canonical Allele Identifier: PA233782
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 166909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056087.2:p.Arg747Gln
CA233780
NM_015272.2:c.2240G>A