Allele Registry

Canonical Allele Identifier: PA2828207856

Gene: NRXN3 HGNC NCBI

ClinVar RCV:

RCV000416434

ClinVar Variation:

375395

HGVS (amino-acid)	Matching Registered Transcripts
NP_001353355.1:p.Lys443Glu	CA16044234 NM_001366426.1:c.1327A>G