Canonical Allele Identifier: PA2827286473
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1315950
ClinVar RCV Id: RCV001757397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317010.1:p.Glu37Gln
CA48054941
NM_001330081.2:c.109G>C