Canonical Allele Identifier: PA2827759425
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Ala1225Pro
CA303346
NM_001353949.2:c.3673G>C