Canonical Allele Identifier: PA2827317501
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 206245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317023.1:p.His841Tyr
CA316137
NM_001330094.2:c.2521C>T