Canonical Allele Identifier: PA2827302271
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1913599
ClinVar RCV Id: RCV002593983
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317016.1:p.Glu99Lys
CA1655529
NM_001330087.2:c.295G>A