Canonical Allele Identifier: PA206248
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 212061
ClinVar RCV Id: RCV000193027 RCV002517127
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121369.1:p.Ala828Asp
CA206247
NM_001127897.1:c.2483C>A