Canonical Allele Identifier: PA2828732101
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 99811
ClinVar RCV Id: RCV000086241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364878.1:p.Asn211Lys
CA227905
NM_001377949.1:c.633T>G
CA388865928
NM_001377949.1:c.633T>A