Canonical Allele Identifier: PA2827302249
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1525587
ClinVar RCV Id: RCV002036800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317016.1:p.Leu89Pro
CA346824350
NM_001330087.2:c.266T>C