Canonical Allele Identifier: PA2827307226
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2089371
ClinVar RCV Id: RCV003005518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317017.1:p.Asn1181Asp
CA346819152
NM_001330088.2:c.3541A>G