Canonical Allele Identifier: PA2827284816
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 950057
ClinVar RCV Id: RCV001221679 RCV002436857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317007.1:p.Ile95Val
CA1655532
NM_001330078.2:c.283A>G