Canonical Allele Identifier: PA2827753051
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Glu1308Asp
CA231476
NM_001353948.2:c.3924A>T
CA349053270
NM_001353948.2:c.3924A>C