Allele Registry

Canonical Allele Identifier: PA2827761023

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000460126

ClinVar Variation:

408926

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340878.1:p.Met1653Thr	CA16610239 NM_001353949.2:c.4958T>C