Canonical Allele Identifier: PA2826258044
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 423370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Leu117Pro
CA16617318
NM_001202435.3:c.350T>C