Canonical Allele Identifier: PA2827320731
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 283768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317024.1:p.Arg742His
CA1654883
NM_001330095.2:c.2225G>A