Canonical Allele Identifier: PA2827287737
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_001317011.1:p.Ser938Ile
CA1654726
NM_001330082.2:c.2813G>T