Canonical Allele Identifier: PA1139740127
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 991022
ClinVar RCV Id: RCV001279156 RCV002493489
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056087.2:p.Ser784Cys
CA395914804
NM_015272.2:c.2351C>G