Allele Registry

Canonical Allele Identifier: PA916036963

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000079588

RCV001823112

ClinVar Variation:

93656

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Met900Thr	CA266846 NM_001353961.2:c.2699T>C