Canonical Allele Identifier: PA2827790261
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189869

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Arg117His
CA303154
NM_001353961.2:c.350G>A