Canonical Allele Identifier: PA2499286020
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1284419
ClinVar RCV Id: RCV001699937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065099.3:p.Pro650Ser
CA388867339
NM_020366.4:c.1948C>T