Canonical Allele Identifier: PA2580311691
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1913599
ClinVar RCV Id: RCV002593983

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004792.1:p.Glu99Lys
CA1655529
NM_004801.6:c.295G>A