Canonical Allele Identifier: PA251695
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1071
ClinVar RCV Id: RCV000001126
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121369.1:p.Ala695Pro
CA251694
NM_001127897.1:c.2083G>C