Canonical Allele Identifier: PA2827284786
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3202225
ClinVar RCV Id: RCV004493637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317007.1:p.Gly74Asp
CA346824439
NM_001330078.2:c.221G>A