Canonical Allele Identifier: PA2827775546
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Thr217Lys
CA285039
NM_001353954.2:c.650C>A