Canonical Allele Identifier: PA658676041
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 449074
ClinVar RCV Id: RCV000522827 RCV000700475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129131.1:p.Asn274Ser
CA1655388
NM_001135659.2:c.821A>G