Canonical Allele Identifier: PA2827753927
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 69406

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Ser1516Leu
CA357173
NM_001353948.2:c.4547C>T