Canonical Allele Identifier: PA2826011464
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 423370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Leu117Pro
CA16617318
NM_001165964.3:c.350T>C