Canonical Allele Identifier: PA2827778945
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 498722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Gln454Lys
CA349070288
NM_001353955.2:c.1360C>A