Canonical Allele Identifier: PA2827284838
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 206236
ClinVar RCV Id: RCV000500819 RCV001041325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317007.1:p.Asp106Asn
CA316121
NM_001330078.2:c.316G>A