Canonical Allele Identifier: PA2827319241
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 206236

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317024.1:p.Asp106Asn
CA316121
NM_001330095.2:c.316G>A