Canonical Allele Identifier: PA2826258413
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189945

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Cys345Arg
CA303376
NM_001202435.3:c.1033T>C