Canonical Allele Identifier: PA170858
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 156380
ClinVar RCV Id: RCV000144462
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.His631Leu
CA170857
NM_020366.4:c.1892A>T