Allele Registry

Canonical Allele Identifier: PA303177

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180827

ClinVar Variation:

189874

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Gln910Lys	CA303174 NM_001165963.4:c.2728C>A