Canonical Allele Identifier: PA2827759687
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Glu1297Asp
CA231476
NM_001353949.2:c.3891A>T
CA349053270
NM_001353949.2:c.3891A>C