Canonical Allele Identifier: PA645425089
Gene: NRTN HGNC NCBI

Linked Data

ClinVar Variation Id: 259427
ClinVar RCV Id: RCV000244407

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004549.1:p.Ala59Thr
CA9117709
NM_004558.5:c.175G>A