Canonical Allele Identifier: PA645501686
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 241026
ClinVar RCV Id: RCV000232122 RCV000271829 RCV000302183 RCV000359252 RCV001271323 RCV004532945
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056087.2:p.Val1188Met
CA8057257
NM_015272.2:c.3562G>A