Canonical Allele Identifier: PA2827284780
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 206230
ClinVar RCV Id: RCV000188259 RCV001852478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317007.1:p.Phe70Leu
CA316109
NM_001330078.2:c.208T>C
CA1655547
NM_001330078.2:c.210C>A
CA346824465
NM_001330078.2:c.210C>G