Canonical Allele Identifier: PA2827288790
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2784660
ClinVar RCV Id: RCV003619971

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317012.1:p.Gly87Ser
CA346824364
NM_001330083.2:c.259G>A