Allele Registry

Canonical Allele Identifier: PA916036987

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000636304

ClinVar Variation:

530440

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Asp941Tyr	CA349068333 NM_001353961.2:c.2821G>T