Canonical Allele Identifier: PA2827784309
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Arg101Trp
CA284919
NM_001353958.2:c.301C>T