Canonical Allele Identifier: PA2827284832
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1946321
ClinVar RCV Id: RCV002658819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317007.1:p.Ala105Thr
CA346824254
NM_001330078.2:c.313G>A