Canonical Allele Identifier: PA2827775456
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206928

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Glu158Gln
CA317752
NM_001353954.2:c.472G>C