Canonical Allele Identifier: PA2827319200
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2650909
ClinVar RCV Id: RCV003407223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317024.1:p.Phe96Cys
CA346824303
NM_001330095.2:c.287T>G