Canonical Allele Identifier: PA2827318306
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1407592
ClinVar RCV Id: RCV001937829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317023.1:p.Asn1240Ser
CA346820186
NM_001330094.2:c.3719A>G