Canonical Allele Identifier: PA2580443707
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2076900
ClinVar RCV Id: RCV002985250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Ser657Phe
CA7089132
NM_020366.4:c.1970C>T