Canonical Allele Identifier: PA2826258404
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 190017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Ala342Ser
CA303563
NM_001202435.3:c.1024G>T