Canonical Allele Identifier: PA303156
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189869

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Arg920His
CA303154
NM_006920.6:c.2759G>A