Canonical Allele Identifier: PA2826012495
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189949

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Ser844Tyr
CA303383
NM_001165964.3:c.2531C>A