Canonical Allele Identifier: PA2827321015
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 2631873
ClinVar RCV Id: RCV004528571

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317467.1:p.Leu250Phe
CA8058038
NM_001330538.2:c.748C>T