Canonical Allele Identifier: PA108202
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68596

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Phe90Ser
CA285078
NM_001165963.4:c.269T>C