Canonical Allele Identifier: PA2573182157
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1476181
ClinVar RCV Id: RCV001977823

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129131.1:p.Gly262Arg
CA346823268
NM_001135659.2:c.784G>C