Canonical Allele Identifier: PA2580146597
Gene: RPTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2389652
ClinVar RCV Id: RCV004231785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116437.1:p.Arg230Gln
CA1099670
NM_001122965.1:c.689G>A