Canonical Allele Identifier: PA2827758357
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Leu886Ser
CA303322
NM_001353949.2:c.2657T>C