Canonical Allele Identifier: PA2827293239
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 206245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317013.1:p.His823Tyr
CA316137
NM_001330084.2:c.2467C>T