Canonical Allele Identifier: PA2825661472
Gene: RPGRIP1L HGNC NCBI

Linked Data

ClinVar Variation Id: 319667
ClinVar RCV Id: RCV000285787 RCV000345463 RCV000396994 RCV002487411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121369.1:p.Gly98Val
CA10647719
NM_001127897.1:c.293G>T