Canonical Allele Identifier: PA2827319208
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1057573
ClinVar RCV Id: RCV001366586
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317024.1:p.Glu99Ala
CA1655528
NM_001330095.2:c.296A>C