Canonical Allele Identifier: PA2826009673
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1474345

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Ile839Thr
CA349062561
NM_001165963.4:c.2516T>C