Canonical Allele Identifier: PA2827285089
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2072711
ClinVar RCV Id: RCV002967309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317007.1:p.Ser297Phe
CA346822603
NM_001330078.2:c.890C>T