Canonical Allele Identifier: PA2825797403
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1315995
ClinVar RCV Id: RCV001757442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129131.1:p.Ser92Gly
CA346824334
NM_001135659.2:c.274A>G