Canonical Allele Identifier: PA2827318193
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1734240
ClinVar RCV Id: RCV002349041 RCV004545294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317023.1:p.Ala1195Val
CA346819205
NM_001330094.2:c.3584C>T