Canonical Allele Identifier: PA2499285991
Gene: RPGRIP1 HGNC NCBI
ClinVar RCV:
RCV001301904
ClinVar Variation:
1005094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Gly29Ser
CA388857088
NM_020366.4:c.85G>A