Canonical Allele Identifier: PA915981133
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 206237
ClinVar RCV Id: RCV000188266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004792.1:p.Arg118His
CA316123
NM_004801.6:c.353G>A