Canonical Allele Identifier: PA2827306538
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 283768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317017.1:p.Arg732His
CA1654883
NM_001330088.2:c.2195G>A