Canonical Allele Identifier: PA2826258443
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Asn359Ser
CA303143
NM_001202435.3:c.1076A>G