Canonical Allele Identifier: PA266113
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Leu1298Phe
CA266111
NM_006920.6:c.3892C>T