Canonical Allele Identifier: PA2827787802
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 93629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Ile407Thr
CA221555
NM_001353960.2:c.1220T>C