Allele Registry

Canonical Allele Identifier: PA2825359450

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV003887086

ClinVar Variation:

3026693

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035233.1:p.Lys1178Met	CA349025769 NM_001040143.2:c.3533A>T