Canonical Allele Identifier: PA2826013086
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 194932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Phe1261Ser
CA241171
NM_001165964.3:c.3782T>C