Canonical Allele Identifier: PA658811983
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 501227
ClinVar RCV Id: RCV000596655 RCV001248488 RCV001330328 RCV001829675 RCV002476328 RCV003278935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056087.2:p.Gln114Arg
CA8058130
NM_015272.2:c.341A>G