Allele Registry

Canonical Allele Identifier: PA2827780889

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000489093

ClinVar Variation:

427080

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340884.1:p.Met1768Val	CA349068113 NM_001353955.2:c.5302A>G