Canonical Allele Identifier: PA2828731759
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1297122
ClinVar RCV Id: RCV001724826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364877.1:p.Pro316Ser
CA388867610
NM_001377948.1:c.946C>T