Canonical Allele Identifier: PA2827321193
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 644164
ClinVar RCV Id: RCV000798024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317024.1:p.Ser929Ile
CA1654726
NM_001330095.2:c.2786G>T