Canonical Allele Identifier: PA2828207856
Gene: NRXN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 375395
ClinVar RCV Id: RCV000416434
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001353355.1:p.Lys443Glu
CA16044234
NM_001366426.1:c.1327A>G