Allele Registry

Canonical Allele Identifier: PA2827780131

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000439959

ClinVar Variation:

383166

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340884.1:p.Cys1342Ser	CA16603838 NM_001353955.2:c.4025G>C CA349050657 NM_001353955.2:c.4024T>A