Allele Registry

Canonical Allele Identifier: PA2829676553

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV002023102

ClinVar Variation:

1512570

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Lys1803del	CA2573133689 NM_006920.6:c.5407_5409del