Canonical Allele Identifier: PA2580311694
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1946321
ClinVar RCV Id: RCV002658819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004792.1:p.Ala105Thr
CA346824254
NM_004801.6:c.313G>A