Canonical Allele Identifier: PA645501462
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 319664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056087.2:p.Tyr362Cys
CA8057930
NM_015272.2:c.1085A>G