Canonical Allele Identifier: PA2826012444
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1474345

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Ile811Thr
CA349062561
NM_001165964.3:c.2432T>C