Canonical Allele Identifier: PA2827779068
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 167646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Arg579Gln
CA234868
NM_001353955.2:c.1736G>A