Canonical Allele Identifier: PA2827774365
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 138982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Ile1454Val
CA295639
NM_001353952.2:c.4360A>G