Canonical Allele Identifier: PA2827298667
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1704104
ClinVar RCV Id: RCV002281439
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317015.1:p.Arg85Cys
CA346824372
NM_001330086.2:c.253C>T