Allele Registry

Canonical Allele Identifier: PA285101

Gene: SCN1A HGNC NCBI

ClinVar Allele:

79497

ClinVar RCV:

RCV000059482

ClinVar Variation:

68605

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Trp941Gly	CA285099 NM_006920.6:c.2821T>G