Canonical Allele Identifier: PA2826011419
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68596

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Phe90Ser
CA285078
NM_001165964.3:c.269T>C