Canonical Allele Identifier: PA2827298706
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1315995
ClinVar RCV Id: RCV001757442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317015.1:p.Ser92Gly
CA346824334
NM_001330086.2:c.274A>G