Canonical Allele Identifier: PA2825797479
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2770860
ClinVar RCV Id: RCV003510408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129131.1:p.Asp106Tyr
CA1655523
NM_001135659.2:c.316G>T