Allele Registry

Canonical Allele Identifier: PA317628

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000189008

RCV001067049

ClinVar Variation:

206870

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Met1856Thr	CA317625 NM_001165963.4:c.5567T>C