Canonical Allele Identifier: PA2827286544
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 206235

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317010.1:p.Arg88Gly
CA316119
NM_001330081.2:c.262C>G