Canonical Allele Identifier: PA2827284821
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1913599
ClinVar RCV Id: RCV002593983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317007.1:p.Glu99Lys
CA1655529
NM_001330078.2:c.295G>A