Canonical Allele Identifier: PA2827296797
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 283768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317014.1:p.Arg750His
CA1654883
NM_001330085.2:c.2249G>A