Canonical Allele Identifier: PA144364
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 56561
ClinVar RCV Id: RCV000049974 RCV002514257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056087.2:p.His610Pro
CA144362
NM_015272.2:c.1829A>C