Canonical Allele Identifier: PA2827766272
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1203729

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Ala1300Val
CA349053215
NM_001353950.2:c.3899C>T