Canonical Allele Identifier: PA2573273494
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1385492
ClinVar RCV Id: RCV001888846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Asp687His
CA257536070
NM_020366.4:c.2059G>C