Canonical Allele Identifier: PA2827314771
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1407592
ClinVar RCV Id: RCV001937829
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317022.1:p.Asn1243Ser
CA346820186
NM_001330093.2:c.3728A>G