Canonical Allele Identifier: PA915977400
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 644164
ClinVar RCV Id: RCV000798024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129131.1:p.Ser986Ile
CA1654726
NM_001135659.2:c.2957G>T