Canonical Allele Identifier: PA2827316465
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2072711
ClinVar RCV Id: RCV002967309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317023.1:p.Ser293Phe
CA346822603
NM_001330094.2:c.878C>T