Canonical Allele Identifier: PA645501371
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 319667
ClinVar RCV Id: RCV000285787 RCV000345463 RCV000396994 RCV002487411
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056087.2:p.Gly98Val
CA10647719
NM_015272.2:c.293G>T