Canonical Allele Identifier: PA2827760515
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 69406

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Ser1505Leu
CA357173
NM_001353949.2:c.4514C>T