Canonical Allele Identifier: PA645478925
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 283768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129131.1:p.Arg790His
CA1654883
NM_001135659.2:c.2369G>A