Allele Registry

Canonical Allele Identifier: PA645429106

Gene: NRXN3 HGNC NCBI

ClinVar RCV:

RCV000416434

ClinVar Variation:

375395

HGVS (amino-acid)	Matching Registered Transcripts
NP_004787.2:p.Lys66Glu	CA16044234 NM_004796.6:c.196A>G