Canonical Allele Identifier: PA108243
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Pro358Thr
CA284856
NM_001165963.4:c.1072C>A