Canonical Allele Identifier: PA2827298734
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1036433
ClinVar RCV Id: RCV001339443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317015.1:p.Glu99Gln
CA346824288
NM_001330086.2:c.295G>C