Canonical Allele Identifier: PA2827773455
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189949

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Ser861Tyr
CA303383
NM_001353952.2:c.2582C>A