Canonical Allele Identifier: PA2827319119
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1023486
ClinVar RCV Id: RCV001323530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317024.1:p.Phe78Leu
CA346824406
NM_001330095.2:c.234C>G
CA346824407
NM_001330095.2:c.234C>A
CA346824412
NM_001330095.2:c.232T>C