Allele Registry

Canonical Allele Identifier: PA916036686

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000478580

RCV003338607

ClinVar Variation:

421777

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Met453Thr	CA16617297 NM_001353961.2:c.1358T>C