Allele Registry

Canonical Allele Identifier: PA2828472519

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000490193

RCV001851317

ClinVar Variation:

427011

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358175.1:p.Ile1473Thr	CA349034225 NM_001371246.1:c.4418T>C