Canonical Allele Identifier: PA2827782624
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 449377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Asp978Glu
CA1943019
NM_001353957.2:c.2934T>G
CA349060373
NM_001353957.2:c.2934T>A