Canonical Allele Identifier: PA2827755986
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 423370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Leu117Pro
CA16617318
NM_001353949.2:c.350T>C