Allele Registry

Canonical Allele Identifier: PA2829675793

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000483132

ClinVar Variation:

421599

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Lys1302Thr	CA16617296 NM_006920.6:c.3905A>C