Canonical Allele Identifier: PA2828731743
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1398945
ClinVar RCV Id: RCV001922690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364877.1:p.Gln291Lys
CA7089128
NM_001377948.1:c.871C>A