Canonical Allele Identifier: PA2828731837
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 438161
ClinVar RCV Id: RCV000504829 RCV001215982 RCV002230986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364877.1:p.Glu442Lys
CA7089253
NM_001377948.1:c.1324G>A