Canonical Allele Identifier: PA2827315756
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 206227

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317023.1:p.Ala101Gly
CA316103
NM_001330094.2:c.302C>G