Canonical Allele Identifier: PA2827288209
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1704104
ClinVar RCV Id: RCV002281439

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317012.1:p.Arg85Cys
CA346824372
NM_001330083.2:c.253C>T