Allele Registry

Canonical Allele Identifier: PA645407741

Gene: SCN2A HGNC NCBI

ClinVar Allele:

362321

ClinVar RCV:

RCV000417035

RCV002521495

ClinVar Variation:

375506

HGVS (amino-acid)	Matching Registered Transcripts
NP_066287.2:p.Met1548Thr	CA16044310 NM_021007.3:c.4643T>C