Canonical Allele Identifier: PA2827305525
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3012423
ClinVar RCV Id: RCV003875550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317017.1:p.Asp106Ala
CA346824250
NM_001330088.2:c.317A>C