Canonical Allele Identifier: PA231478
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Glu1297Asp
CA231476
NM_006920.6:c.3891A>T
CA349053270
NM_006920.6:c.3891A>C