Allele Registry

Canonical Allele Identifier: PA916037005

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059444

RCV001854242

ClinVar Variation:

68569

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Met966Thr	CA285018 NM_001353961.2:c.2897T>C