Canonical Allele Identifier: PA2827303707
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 283768
ClinVar RCV Id: RCV000287218 RCV001855131
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317016.1:p.Arg722His
CA1654883
NM_001330087.2:c.2165G>A