Canonical Allele Identifier: PA2827759369
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1475150

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Phe1215Val
CA349055801
NM_001353949.2:c.3643T>G