Canonical Allele Identifier: PA2825661944
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1351355
ClinVar RCV Id: RCV002044662 RCV002489938 RCV003247047
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121369.1:p.Lys706Asn
CA8057638
NM_001127897.1:c.2118A>C
CA395916602
NM_001127897.1:c.2118A>T