Allele Registry

Canonical Allele Identifier: PA2829675862

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000439959

ClinVar Variation:

383166

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Cys1343Ser	CA16603838 NM_006920.6:c.4028G>C CA349050657 NM_006920.6:c.4027T>A