Canonical Allele Identifier: PA2827286958
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1318649
ClinVar RCV Id: RCV001768273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317011.1:p.Thr102Ala
CA346824271
NM_001330082.2:c.304A>G