Canonical Allele Identifier: PA2827288776
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1040105
ClinVar RCV Id: RCV001343689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317012.1:p.Gly74Ala
CA346824438
NM_001330083.2:c.221G>C