Canonical Allele Identifier: PA1139688441
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 930930
ClinVar RCV Id: RCV001196942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129131.1:p.Lys286Glu
CA346823040
NM_001135659.2:c.856A>G