Canonical Allele Identifier: PA2827786831
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68570

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Ala1755Thr
CA285021
NM_001353958.2:c.5263G>A