Canonical Allele Identifier: PA2827300765
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1516979
ClinVar RCV Id: RCV002027003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317015.1:p.Ser946Asn
CA346776770
NM_001330086.2:c.2837G>A