Allele Registry

Canonical Allele Identifier: PA2828207784

Gene: NRXN3 HGNC NCBI

ClinVar RCV:

RCV000416434

ClinVar Variation:

375395

HGVS (amino-acid)	Matching Registered Transcripts
NP_001353354.1:p.Lys439Glu	CA16044234 NM_001366425.1:c.1315A>G