Canonical Allele Identifier: PA2573266317
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1436544
ClinVar RCV Id: RCV001974790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056087.2:p.Thr795Ala
CA395914738
NM_015272.2:c.2383A>G