Canonical Allele Identifier: PA916036700
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Leu473Pro
CA285150
NM_001353961.2:c.1418T>C