Canonical Allele Identifier: PA303324
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Leu886Ser
CA303322
NM_006920.6:c.2657T>C