Canonical Allele Identifier: PA2827288466
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 283768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317012.1:p.Arg737His
CA1654883
NM_001330083.2:c.2210G>A