Canonical Allele Identifier: PA2580146616
Gene: RPTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2458636
ClinVar RCV Id: RCV004248907

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001116437.1:p.Lys735Glu
CA1099343
NM_001122965.1:c.2203A>G