Canonical Allele Identifier: PA2826258194
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Thr217Lys
CA285039
NM_001202435.3:c.650C>A